Detection of clinically relevant exonic copy‐number changes by array CGH

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Human Mutation

• Publication date

  2010-12-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/humu.21360PMID 20848651PMCID PMC3158569
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Exon deletions of the EP300 and CREBBP genes in two children with Rubinstein–Taybi syndrome detected by aCGH

  2011cited by this paper
• Disruption of the SCN2A and SCN3A genes in a patient with mental retardation, neurobehavioral and psychiatric abnormalities, and a history of infantile seizures

  2011cited by this paper
• Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

  2010influential reference
• Copy number variation upstream of PMP22 in Charcot–Marie–Tooth disease

  2010cited by this paper
• Origins and functional impact of copy number variation in the human genome

  2010cited by this paper
• Structural variation in the human genome and its role in disease.

  2010cited by this paper
• Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay.

  2010cited by this paper
• Mechanisms for nonrecurrent genomic rearrangements associated with CMT1A or HNPP: rare CNVs as a cause for missing heritability.

  2010cited by this paper
• Identification of uncommon recurrent Potocki-Lupski syndrome-associated duplications and the distribution of rearrangement types and mechanisms in PTLS.

  2010cited by this paper
• Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies

  2010cited by this paper
• HERV‐mediated genomic rearrangement of EYA1 in an individual with branchio‐oto‐renal syndrome

  2010cited by this paper
• A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay

  2010cited by this paper
• Rare mutations of FGFR2 causing apert syndrome: identification of the first partial gene deletion, and an Alu element insertion from a new subfamily

  2009cited by this paper
• Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping

  2009cited by this paper
• Intragenic deletion of TRIM32 in compound heterozygotes with sarcotubular myopathy/LGMD2H

  2009cited by this paper
• Human copy number polymorphic genes

  2009cited by this paper
• [Structural variation in the human genome].

  2009cited by this paper
• Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.

  2009cited by this paper
• A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

  2009cited by this paper
• Dominant versus recessive traits conveyed by allelic mutations – to what extent is nonsense‐mediated decay involved?

  2009cited by this paper
• A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

  2009cited by this paper
• De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy

  2009cited by this paper
• Targeted comparative genomic hybridization array for the detection of single- and multiexon gene deletions and duplications

  2009cited by this paper
• Alu-specific microhomology-mediated deletions in CDKL5 in females with early-onset seizure disorder

  2009cited by this paper
• Genomic disorders ten years on

  2009cited by this paper
• Mechanisms of change in gene copy number

  2009cited by this paper
• Duplication hotspots, rare genomic disorders, and common disease.

  2009cited by this paper
• Complex human chromosomal and genomic rearrangements.

  2009cited by this paper
• The DNA replication FoSTeS/MMBIR mechanism can generate genomic, genic and exonic complex rearrangements in humans

  2009cited by this paper
• Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

  2009cited by this paper
• Genomic Imbalances in Neonates With Birth Defects: High Detection Rates by Using Chromosomal Microarray Analysis

  2008cited by this paper
• Detection and precise mapping of germline rearrangements in BRCA1, BRCA2, MSH2, and MLH1 using zoom‐in array comparative genomic hybridization (aCGH)

  2008cited by this paper
• Mutations in the cyclin family member FAM58A cause an X-linked dominant disorder characterized by syndactyly, telecanthus and anogenital and renal malformations

  2008cited by this paper
• Mechanisms for human genomic rearrangements

  2008cited by this paper
• Utility of oligonucleotide array-based comparative genomic hybridization for detection of target gene deletions.

  2008cited by this paper
• Microarray‐based mutation detection in the dystrophin gene

  2008cited by this paper
• Brief Report: Autistic Symptoms, Developmental Regression, Mental Retardation, Epilepsy, and Dyskinesias in CNS Folate Deficiency

  2008cited by this paper
• Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: A study of 5,380 cases

  2008cited by this paper
• A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies

  2008cited by this paper
• Detection of exonic copy‐number changes using a highly efficient oligonucleotide‐based comparative genomic hybridization‐array method

  2008cited by this paper
• Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

  2008cited by this paper
• Alternative Splicing in Colon, Bladder, and Prostate Cancer Identified by Exon Array Analysis*S

  2008cited by this paper
• Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses

  2008cited by this paper
• Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array‐comparative genomic hybridization

  2008cited by this paper
• Structural variation in the human genome.

  2007cited by this paper
• Alternative Splicing Events Identified in Human Embryonic Stem Cells and Neural Progenitors

  2007cited by this paper
• Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.

  2007cited by this paper
• Discovery of tissue-specific exons using comprehensive human exon microarrays

  2007cited by this paper
• A DNA replication mechanism for generating nonrecurrent rearrangements associated with genomic disorders.

  2007cited by this paper
• Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases

  2007cited by this paper
• Male-to-female sex reversal associated with an ∼250 kb deletion upstream of NR0B1 (DAX1)

  2007cited by this paper
• Microarray‐based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics

  2007cited by this paper
• Male-to-female sex reversal associated with an approximately 250 kb deletion upstream of NR0B1 (DAX1).

  2007cited by this paper
• Exon arrays provide accurate assessments of gene expression

  2007cited by this paper
• Global variation in copy number in the human genome

  2006cited by this paper
• Expression of distinct classes of titin isoforms in striated and smooth muscles by alternative splicing, and their conserved interaction with filamins.

  2006cited by this paper
• Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect

  2006cited by this paper
• Alternative splicing and differential gene expression in colon cancer detected by a whole genome exon array

  2006cited by this paper
• Genomic Disorders: Molecular Mechanisms for Rearrangements and Conveyed Phenotypes

  2005cited by this paper
• Cerebral folate deficiency with developmental delay, autism, and response to folinic acid

  2005cited by this paper
• Phenotypic consequences of genetic variation at hemizygous alleles: Sotos syndrome is a contiguous gene syndrome incorporating coagulation factor twelve (FXII) deficiency

  2005cited by this paper
• Development and validation of a CGH microarray for clinical cytogenetic diagnosis

  2005cited by this paper
• DHHC9 and GCP16 Constitute a Human Protein Fatty Acyltransferase with Specificity for H- and N-Ras*

  2005cited by this paper
• Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.

  2005cited by this paper
• Large-Scale Copy Number Polymorphism in the Human Genome

  2004cited by this paper
• Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations

  2004cited by this paper
• Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders

  2004cited by this paper
• Mutation analysis of the tumor suppressor PTEN and the glypican 3 (GPC3) gene in patients diagnosed with Proteus syndrome

  2004cited by this paper
• Detection of large-scale variation in the human genome

  2004cited by this paper
• Molecular mechanisms for genomic disorders.

  2003cited by this paper
• An ABCA4 genomic deletion in patients with Stargardt disease

  2003cited by this paper
• Gross rearrangements in the MECP2 gene in three patients with rett syndrome: Implications for routine diagnosis of Rett syndrome

  2003cited by this paper
• Genome architecture, rearrangements and genomic disorders.

  2002cited by this paper
• Nonsense-associated altered splicing: a frame-dependent response distinct from nonsense-mediated decay.

  2002cited by this paper
• Intron-size constraint as a mutational mechanism in Rothmund-Thomson syndrome.

  2002cited by this paper
• Germline mutation of the tumour suppressor PTEN in Proteus syndrome

  2002cited by this paper
• PTEN mutations and proteus syndrome.

  2001cited by this paper
• The 1.4-Mb CMT1A duplication/HNPP deletion genomic region reveals unique genome architectural features and provides insights into the recent evolution of new genes.

  2001cited by this paper
• PTEN mutations are uncommon in Proteus syndrome.

  2001cited by this paper
• Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes.

  2001cited by this paper
• An atypical intronic deletion widens the spectrum of mutations in hereditary spastic paraplegia

  2001influential reference
• DNA rearrangements on both homologues of chromosome 17 in a mildly delayed individual with a family history of autosomal dominant carpal tunnel syndrome.

  1999cited by this paper
• Genomic disorders: structural features of the genome can lead to DNA rearrangements and human disease traits.

  1998cited by this paper
• Germline mutations in PTEN are present in Bannayan-Zonana syndrome

  1997influential reference
• Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

  1997influential reference
• Diagnosis of CMT1A duplications and HNPP deletions by interphase FISH: implications for testing in the cytogenetics laboratory.

  1997cited by this paper
• An autosomal dominant syndrome of renal and anogenital malformations with syndactyly.

  1996cited by this paper
• When cells stop making sense: effects of nonsense codons on RNA metabolism in vertebrate cells.

  1995cited by this paper
• Deletion of 19 base pairs in intron 13 of the gene for the proα2(I) chain of type-I procollagen (COL1A2) causes exon skipping in a proband with type-I osteogenesis imperfecta

  1993influential reference
• The skipping of constitutive exons in vivo induced by nonsense mutations

  1993cited by this paper
• The chimeric gene linked to glucocorticoid-suppressible hyperaldosteronism encodes a fused P-450 protein possessing aldosterone synthase activity.

  1992cited by this paper
• Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

  1992cited by this paper
• A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

  1992cited by this paper
• Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families.

  1990cited by this paper
• Alu-Alu recombination deletes splice acceptor sites and produces secreted low density lipoprotein receptor in a subject with familial hypercholesterolemia.

  1987cited by this paper
• Sickle-cell trait as a risk factor for sudden death in physical training.

  1987cited by this paper
• Splenic syndrome at mountain altitudes in sickle cell trait. Its occurrence in nonblack persons.

  1985cited by this paper
• Molecular evidence for new mutation at the hprt locus in Lesch-Nyhan patients

  1984cited by this paper
• Expression of the Familial Hypercholesterolemia Gene in Heterozygotes: Mechanism for a Dominant Disorder in Man

  1974cited by this paper

• Computationally resolved neuroprogenitor cell biomarkers associate with human disorders

  2025cites this paper
• Toe Polydactyly and Supernumerary Nipple: Broadening the Phenotypic Spectrum of STAR Syndrome

  2025cites this paper
• Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage.

  2025cites this paper
• FGFR Aberrations in Solid Tumors: Mechanistic Insights and Clinical Translation of Targeted Therapies

  2025cites this paper
• Chromosomal abnormalities in primary and secondary recurrent miscarriages: significance for PGT-A

  2025cites this paper
• Application of genome and exome sequencing to study craniofacial conditions – A Primer

  2024cites this paper
• The X‐Linked Intellectual Disability Gene, ZDHHC9 , Is Important for Oligodendrocyte Subtype Determination and Myelination

  2024cites this paper
• Homozygous Intragenic Deletion in WDR62 in Siblings with Primary Microcephaly

  2024cites this paper
• Auricular fistula: a review of its clinical manifestations, genetics, and treatments

  2023cites this paper
• SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability

  2023cites this paper
• HMZDupFinder: a robust computational approach for detecting intragenic homozygous duplications from exome sequencing data

  2023cites this paper
• The X-Linked Intellectual Disability gene, ZDHHC9 , is important for oligodendrocyte maturation and myelin formation

  2023cites this paper
• Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature

  2023cites this paper
• Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences

  2022cites this paper
• High‐level gonosomal mosaicism for a pathogenic non‐coding CNV deletion of the lung‐specific FOXF1 enhancer in an unaffected mother of an infant with ACDMPV

  2022cites this paper
• Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome

  2022cites this paper
• Detection of the Copy Number Variants of Genes in Patients with Familial Cardiac Diseases by Massively Parallel Sequencing

  2022cites this paper
• TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.

  2022cites this paper
• ZDHHC9 X‐linked intellectual disability: Clinical and molecular characterization

  2022cites this paper
• HSD17B12 dosage insufficiency induced premature ovarian insufficiency in humans and mice

  2022cites this paper
• Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptom

  2022cites this paper
• The identification of a novel CCNQ gene tail extension variant contributing to syndactyly, telecanthus and anogenital and renal malformations syndrome

  2022cites this paper
• CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and Limitations

  2021cites this paper
• IL1RAPL1 Gene Deletion in a Female Patient with Developmental Delay and Continuous Spike-Wave during Sleep

  2021cites this paper
• Somatic mosaicism in inherited bone marrow failure and chromosomal instability syndrome

  2021cites this paper
• Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset

  2021cites this paper
• Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings

  2021cites this paper
• Expanding the phenotype associated with interstitial 6p25.1p24.3 microdeletion: a new case and review of the literature

  2021cites this paper
• Cilia kinases in skeletal development and homeostasis

  2021cites this paper
• Transcriptome analysis of MBD5-associated neurodevelopmental disorder (MAND) neural progenitor cells reveals dysregulation of autism-associated genes

  2021cites this paper
• Cyclin-Dependent Kinases (CDK) and Their Role in Diseases Development–Review

  2021cites this paper
• Exome sequencing as a first-tier test for copy number variant detection: retrospective evaluation and prospective screening in 2418 cases

  2021cites this paper
• CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank

  2021cites this paper
• CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

  2020cites this paper
• New Insights into Potocki-Shaffer Syndrome: Report of Two Novel Cases and Literature Review

  2020cites this paper
• Copy number alterations involving 59 ACMG‐recommended secondary findings genes

  2020cites this paper
• Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditions

  2020cites this paper
• Optimizing Genetic Diagnosis of Neurodevelopmental Disorders in the Clinical Setting.

  2020cites this paper
• Cyclin-dependent kinases and rare developmental disorders

  2020cites this paper
• Low-level parental somatic mosaic SNVs in exomes from a large cohort of trios with diverse suspected Mendelian conditions

  2020cites this paper
• Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres

  2020cites this paper
• Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.

  2020cites this paper
• CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indels

  2020cites this paper
• Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settings.

  2020cites this paper
• Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.

  2020cites this paper
• De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndrome

  2019cites this paper
• Combinations of exonic deletions and rare mutations lead to misdiagnosis of propionic acidemia.

  2019cites this paper
• Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child.

  2019cites this paper
• Molecular analysis of glycosylphosphatidylinositol anchor deficient aerolysin resistant isolates in gulf war i veterans exposed to depleted uranium

  2019influential citation
• Genetic architecture of laterality defects revealed by whole exome sequencing

  2019cites this paper
• Insights into genetics, human biology and disease gleaned from family based genomic studies

  2019cites this paper
• Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders

  2019cites this paper
• Importance of patient selection criteria in determining diagnostic copy number variations in patients with multiple congenital anomaly/mental retardation

  2019cites this paper
• Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases

  2019cites this paper
• Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype–phenotype correlations

  2019cites this paper
• Mutations in Mediator Complex Genes CDK8, MED12, MED13, and MEDL13 Mediate Overlapping Developmental Syndromes

  2019cites this paper
• Novel applications of array comparative genomic hybridization in molecular diagnostics

  2018cites this paper
• Copy Number Variation.

  2018cites this paper
• Expanding the molecular basis and phenotypic spectrum of ZDHHC9‐associated X‐linked intellectual disability

  2018cites this paper
• TASP1 is deleted in an infant with developmental delay, microcephaly, distinctive facial features, and multiple congenital anomalies

  2018cites this paper
• Intragenic Deletions May Involve Enhancer Sequences and Alter CNTNAP2 Expression

  2018cites this paper
• Bioinformatic Approaches to Detecting Copy Number Variation in Next Generation Sequencing Data for Clinical Diagnostics

  2018cites this paper
• Phenotypic association of 15q11.2 CNVs of the region of breakpoints 1–2 (BP1–BP2) in a large cohort of samples referred for genetic diagnosis

  2018cites this paper
• Fetal nucleic acids in maternal plasma: from biology to clinical translation.

  2018cites this paper
• TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice

  2018cites this paper
• Copy Number Variants of Undetermined Significance Are Not Associated with Worse Clinical Outcomes in Hypoplastic Left Heart Syndrome

  2018cites this paper
• NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders

  2018cites this paper
• A comprehensive clinical and genetic study in 127 patients with ID in Kinshasa, DR Congo

  2018cites this paper
• Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions

  2018cites this paper
• Whole-exome sequencing reveals SALL 4 variants in premature ovarian insufficiency : an update on genotype – phenotype correlations

  2018cites this paper
• Structural Genome Variations Related to Craniosynostosis

  2018cites this paper
• au Array-Comparative Genomic Hybridization Reveals Loss of SOCS 6 Is Associated with Poor Prognosis in Primary Lung Squamous Cell Carcinoma

  2017cites this paper
• The awakening of the CDK10/Cyclin M protein kinase

  2017cites this paper
• Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach

  2017cites this paper
• Array-Comparative Genomic Hybridization/Microarray Analysis: Interpretation of Copy Number Variants

  2017cites this paper
• Evaluation of three read-depth based CNV detection tools using whole-exome sequencing data

  2017cites this paper
• What Mutagenic Events Contribute to Human Cancer and Genetic Disease

  2017cites this paper
• Genomic microarray technologies for the cytogenetics laboratory

  2017cites this paper
• The first patient with sporadic X-linked intellectual disability with de novo ZDHHC9 mutation identified by targeted next-generation sequencing.

  2017cites this paper
• Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features.

  2017cites this paper
• Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotype

  2017influential citation
• Copy Number Variation Disorders

  2017cites this paper
• WISExome: a within-sample comparison approach to detect copy number variations in whole exome sequencing data

  2017cites this paper
• Clinical interpretation of copy number variants in the human genome

  2017cites this paper
• De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder.

  2017cites this paper
• STAR syndrome plus: The first description of a female patient with the lethal form

  2017influential citation
• Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features

  2017cites this paper
• Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant Validation

  2017cites this paper
• STAR syndrome: a further case and the first report of maternal mosaicism.

  2017cites this paper
• The importance of phase analysis in multiexon copy number variation detected by aCGH in autosomal recessive disorder loci

  2017cites this paper
• Identification of novel candidate disease genes from de novo exonic copy number variants

  2017influential citation
• Genetic counselling difficulties and ethical implications of incidental findings from array‐CGH: a 7‐year national survey

  2016cites this paper
• A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson’s disease

  2016cites this paper
• Copy number analysis of the low-copy repeats at the primate NPHP1 locus by array comparative genomic hybridization

  2016cites this paper
• Genetics of Parkinson’s Disease: The Role of Copy Number Variations

  2016cites this paper
• CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

  2016cites this paper
• Somatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjects.

  2016cites this paper
• Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome.

  2016cites this paper
• Copy number variation as a genetic basis for heterotaxy and heterotaxy-spectrum congenital heart defects

  2016cites this paper
• Amitosis generates differentiated cell nuclei from chomatin 1 mass formed after monolayer nuclei are aggregated , beome 2 pyknotic , and are fragmented : Differentiation of Epithelial 3 Domes

  2016cites this paper