The genetics of isolated orofacial clefts: from genotypes to subphenotypes.

No abstract is available for this paper.

• Publication year

  2009

• Venue

  Oral Diseases

• Publication date

  2009-10-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1111/j.1601-0825.2009.01577.xPMID 19583827
• 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.

• Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome

  2009cited by this paper
• Genetic Determinants of Facial Clefting: Analysis of 357 Candidate Genes Using Two National Cleft Studies from Scandinavia

  2009cited by this paper
• The PDGF-C regulatory region SNP rs28999109 decreases promoter transcriptional activity and is associated with CL/P

  2009cited by this paper
• Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip.

  2009cited by this paper
• Hand2 is required in the epithelium for palatogenesis in mice.

  2009cited by this paper
• Biological Mechanisms in Palatogenesis and Cleft Palate

  2009cited by this paper
• Interactions between TGF-beta1 and TGF-beta3 and their role in medial edge epithelium cell death and palatal fusion in vitro.

  2009cited by this paper
• Genome Scan, Fine-Mapping, and Candidate Gene Analysis of Non-Syndromic Cleft Lip with or without Cleft Palate Reveals Phenotype-Specific Differences in Linkage and Association Results

  2009cited by this paper
• Identification of microdeletions in candidate genes for cleft lip and/or palate.

  2009cited by this paper
• Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24

  2009cited by this paper
• Mouse genetic models of cleft lip with or without cleft palate.

  2008cited by this paper
• Missense mutations that cause Van der Woude syndrome and popliteal pterygium syndrome affect the DNA-binding and transcriptional activation functions of IRF6

  2008cited by this paper
• Dental Anomalies as Part of the Cleft Spectrum

  2008cited by this paper
• Familial risk of oral clefts by morphological type and severity: population based cohort study of first degree relatives

  2008cited by this paper
• Disruption of an AP-2α binding site in an IRF6 enhancer is strongly associated with cleft lip

  2008cited by this paper
• The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models.

  2008cited by this paper
• MicroRNA Mirn140 modulates Pdgf signaling during palatogenesis

  2008cited by this paper
• Incidence of Neurological Soft Signs in Children with Isolated Cleft of the Lip or Palate

  2008cited by this paper
• Three‐dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: A possible marker for genetic susceptibility

  2008cited by this paper
• TFAP2A mutations result in branchio-oculo-facial syndrome.

  2008cited by this paper
• Mice with an anterior cleft of the palate survive neonatal lethality

  2008cited by this paper
• Rethinking isolated cleft palate: Evidence of occult lip defects in a subset of cases

  2008cited by this paper
• Genetic variants in IRF6 and the risk of facial clefts: single‐marker and haplotype‐based analyses in a population‐based case‐control study of facial clefts in Norway

  2008cited by this paper
• The Mn1 transcription factor acts upstream of Tbx22 and preferentially regulates posterior palate growth in mice

  2008cited by this paper
• Alteration of medial-edge epithelium cell adhesion in two Tgf-β3 null mouse strains

  2008cited by this paper
• Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project.

  2008cited by this paper
• Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions.

  2007cited by this paper
• The development of the neural crest in the human

  2007cited by this paper
• Social function in boys with cleft lip and palate: relationship to ventral frontal cortex morphology.

  2007cited by this paper
• Orbicularis oris muscle defects as an expanded phenotypic feature in nonsyndromic cleft lip with or without cleft palate

  2007cited by this paper
• CRISPLD2: a novel NSCLP candidate gene.

  2007cited by this paper
• Sequence evaluation of FGF and FGFR gene conserved non‐coding elements in non‐syndromic cleft lip and palate cases

  2007cited by this paper
• Abnormal brain structure in children with isolated clefts of the lip or palate.

  2007cited by this paper
• FGF signalling and SUMO modification: new players in the aetiology of cleft lip and/or palate.

  2007cited by this paper
• Molecular control of secondary palate development.

  2007cited by this paper
• Abnormal brain structure in adults with Van der Woude syndrome

  2007cited by this paper
• TBX22 mutations are a frequent cause of non‐syndromic cleft palate in the Thai population

  2007cited by this paper
• Defining Subphenotypes for Oral Clefts Based on Dental Development

  2007cited by this paper
• Subclinical features in non-syndromic cleft lip with or without cleft palate (CL/P): review of the evidence that subepithelial orbicularis oris muscle defects are part of an expanded phenotype for CL/P.

  2007cited by this paper
• TBX22 missense mutations found in patients with X-linked cleft palate affect DNA binding, sumoylation, and transcriptional repression.

  2007cited by this paper
• p63-Associated Disorders

  2007cited by this paper
• Interferon regulatory factor 6 (IRF6) and fibroblast growth factor receptor 1 (FGFR1) contribute to human tooth agenesis

  2007cited by this paper
• Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.

  2007cited by this paper
• Impaired FGF signaling contributes to cleft lip and palate

  2007cited by this paper
• Palatal fusion - where do the midline cells go? A review on cleft palate, a major human birth defect.

  2007cited by this paper
• Association between the transforming growth factor alpha gene and nonsyndromic oral clefts: a HuGE review.

  2006cited by this paper
• SUMO: regulating the regulator

  2006cited by this paper
• PDGF-C controls proliferation and is down-regulated by retinoic acid in mouse embryonic palatal mesenchymal cells.

  2006cited by this paper
• Analysis of candidate genes on chromosome 2 in oral cleft case-parent trios from three populations

  2006cited by this paper
• FGF signalling in craniofacial development and developmental disorders.

  2006cited by this paper
• The Pittsburgh Oral-Facial Cleft Study: Expanding the Cleft Phenotype. Background and Justification

  2006cited by this paper
• Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch

  2006cited by this paper
• Wnt/beta-catenin signaling in development and disease.

  2006cited by this paper
• Mutations in WNT7A cause a range of limb malformations, including Fuhrmann syndrome and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome.

  2006cited by this paper
• Holoprosencephaly: clinical, anatomic, and molecular dimensions.

  2006cited by this paper
• Developmental expression analysis of the mouse and chick orthologues of IRF6: The gene mutated in Van der Woude syndrome

  2006cited by this paper
• Contributions of PTCH Gene Variants to Isolated Cleft Lip and Palate

  2006cited by this paper
• Development of the upper lip: Morphogenetic and molecular mechanisms

  2006cited by this paper
• Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome

  2006cited by this paper
• Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)

  2006cited by this paper
• PVRL1 variants contribute to non‐syndromic cleft lip and palate in multiple populations

  2006cited by this paper
• Human Genome Epidemiology (HuGE) Review Association between the Transforming Growth Factor Alpha Gene and Nonsyndromic Oral Clefts: A HuGE Review

  2006cited by this paper
• A mutation of the p63 gene in non-syndromic cleft lip

  2006cited by this paper
• SUMO1 Haploinsufficiency Leads to Cleft Lip and Palate

  2006cited by this paper
• Parental craniofacial morphology in cleft lip with or without cleft palate as determined by cephalometry: a meta-analysis.

  2006cited by this paper
• Candidate Genes for Oral-Facial Clefts in Guatemalan Families

  2006cited by this paper
• Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test.

  2006cited by this paper
• Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate

  2005cited by this paper
• Identification of Markers of the Midface

  2005cited by this paper
• Threshold-specific requirements for Bmp4 in mandibular development.

  2005cited by this paper
• Gene expression in pharyngeal arch 1 during human embryonic development.

  2005cited by this paper
• Progress toward discerning the genetics of cleft lip

  2005cited by this paper
• BMP signaling in skeletal development.

  2005cited by this paper
• Genomic, cDNA and embryonic expression analysis of zebrafish IRF6, the gene mutated in the human oral clefting disorders Van der Woude and popliteal pterygium syndromes.

  2005cited by this paper
• Orofacial clefting: recent insights into a complex trait.

  2005cited by this paper
• Distinct functions for Bmp signaling in lip and palate fusion in mice

  2005cited by this paper
• The cellular and molecular etiology of the cleft secondary palate in Fgf10 mutant mice.

  2005cited by this paper
• Wnt9b plays a central role in the regulation of mesenchymal to epithelial transitions underlying organogenesis of the mammalian urogenital system.

  2005cited by this paper
• Cleft lip and palate versus cleft lip only: are they distinct defects?

  2005cited by this paper
• TBX22 mutations are a frequent cause of cleft palate

  2004cited by this paper
• Developmental gene expression profiling of mammalian, fetal orofacial tissue.

  2004cited by this paper
• Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous family.

  2004cited by this paper
• Signal transduction of bone morphogenetic protein receptors.

  2004cited by this paper
• Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35.

  2004cited by this paper
• MSX1, PAX9, and TGFA Contribute to Tooth Agenesis in Humans

  2004cited by this paper
• Hedgehog signaling in the neural crest cells regulates the patterning and growth of facial primordia.

  2004cited by this paper
• Perspectives on growth factors and orofacial development.

  2004cited by this paper
• Cleft palate: players, pathways, and pursuits.

  2004cited by this paper
• A digenic cause of cleft lip in A-strain mice and definition of candidate genes for the two loci.

  2004cited by this paper
• Transforming growth factor β (TGFβ) signalling in palatal growth, apoptosis and epithelial mesenchymal transformation (EMT)

  2004cited by this paper
• Long term follow up study of survival associated with cleft lip and palate at birth

  2004cited by this paper
• A specific requirement for PDGF-C in palate formation and PDGFR-α signaling

  2004cited by this paper
• A specific requirement for PDGF-C in palate formation and PDGFR-alpha signaling.

  2004cited by this paper
• Transforming growth factor beta (TGFbeta) signalling in palatal growth, apoptosis and epithelial mesenchymal transformation (EMT).

  2004cited by this paper
• Genetic approaches to identify disease genes for birth defects with cleft lip/palate as a model.

  2004cited by this paper
• Disruption of Fgf10/Fgfr2b-coordinated epithelial-mesenchymal interactions causes cleft palate.

  2004cited by this paper
• Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate.

  2004cited by this paper
• The cleft lip and palate defects in Dancer mutant mice result from gain of function of the Tbx10 gene.

  2004cited by this paper
• Requirement of the forkhead gene Foxe1, a target of sonic hedgehog signaling, in hair follicle morphogenesis.

  2004cited by this paper
• Genetic Association Studies of Cleft Lip and/or Palate with Hypodontia outside the Cleft Region

  2003cited by this paper

• Advancements in Pathogenic Genes and Biomarkers for Non-syndromic Cleft Lip With or Without Cleft Palate Via Multiomics

  2025cites this paper
• Novel insights into palatal shelf elevation dynamics in normal mouse embryos

  2025cites this paper
• Association of ABCA4 gene polymorphisms with nonsyndromic cleft lip with or without cleft palate in a case-parent trio study.

  2025cites this paper
• PRMT1-methylated MSX1 phase separates to control palate development

  2025cites this paper
• Expression analysis of genes including Zfhx4 in mice and zebrafish reveals a temporospatial conserved molecular basis underlying craniofacial development

  2024cites this paper
• Congenital cardiac anomalies in non‐syndromic cleft lip and cleft palate patients: A systematic review and meta‐analysis

  2024cites this paper
• Craniofacial Cephalometric Morphology in Polish Adolescents with Cleft Palate Only

  2024cites this paper
• The application of zebrafish model in the study of cleft lip and palate development: A systematic review

  2024cites this paper
• Evaluation of facial pleasantness in patients with complete and unilateral cleft lip and palate rehabilitated and submitted to orofacial harmonization

  2024cites this paper
• Single-Nucleotide Polymorphisms in WNT Genes in Patients with Non-Syndromic Orofacial Clefts in a Polish Population

  2024cites this paper
• Genetic Variability of IRF6 Polymorphisms in Non-Syndromic Cleft Lip/Palate: A Meta-Analysis Across Diverse Populations

  2024cites this paper
• Identification of Novel Risk Variants of Non-Syndromic Cleft Palate by Targeted Gene Panel Sequencing

  2023cites this paper
• Origini, forma e (dis)funzioni dell’apparato masticatorio in Homo sapiens 

  2023cites this paper
• Isolated nonsyndromic cleft palate: multicenter epidemiological study in the Brazil

  2023cites this paper
• Maternal Transmission of the PAX7 Single Nucleotide Polymorphisms among Indian Cleft Trios

  2023cites this paper
• Cleft palate in fetuses: feasibility of early diagnosis by Crystal and Realistic Vue rendering 3D ultrasound technology in the first trimester

  2023cites this paper
• Association between IRF6, TP63, GREM1 Gene Polymorphisms and Non-Syndromic Orofacial Cleft Phenotypes in Vietnamese Population: A Case–Control and Family-Based Study

  2023cites this paper
• A mutational hotspot in AMOTL1 defines a new syndrome of orofacial clefting, cardiac anomalies, and tall stature

  2023cites this paper
• The relationship between maternal periconceptional micronutrient supplementation and non‐syndromic cleft lip/palate in offspring

  2023cites this paper
• Comparison of Presurgical Anthropometric Measures of Right and Left Complete Unilateral Cleft Lip and/or Palate

  2022cites this paper
• Novel insights into the fundamentals of palatal shelf elevation dynamics in normal mouse embryos

  2022cites this paper
• Identification of a novel missense mutation in non-syndromic familial multiple supernumerary teeth.

  2022cites this paper
• Cross-Linked Hyaluronic Acid for Cleft Lip and Palate Aesthetic Correction: A Preliminary Report

  2022cites this paper
• MicroRNAs as epigenetic regulators of orofacial development.

  2022cites this paper
• Association of single nucleotide polymorphisms in the IRF6 gene with nonsyndromic cleft lip with or without cleft palate in Kinh Vietnamese patients

  2022influential citation
• Differential expression of the IRF6 gene in the signs of Van der Woude Syndrome: Are distinct genetic modifiers operating?

  2021cites this paper
• The Geographical Factors in Cleft Lip and Cleft Palate among Infants as Congenital Anomalies over West Bengal: A Systematic Review and Meta-Analysis

  2021cites this paper
• Cleft Lip and Palate

  2021cites this paper
• Sendromik Olmayan Konjenital Yarık Damak-Dudak Bulunan Hastalarda Kopya Sayısı Varyasyonlarının Belirlenmesi

  2021cites this paper
• Homozygous deletion of glutathione S-transferase theta 1 and mu 1 increase the risk of non-syndromic oral clefts in a Mexican population.

  2021cites this paper
• Prospective cohort study to evaluate narrow diameter implants for restoration of a missing lateral incisor in patients with a cleft palate: One-year results.

  2021cites this paper
• Exosomes—a potential indicator and mediator of cleft lip and palate: a narrative review

  2021cites this paper
• Dental Subphenotypes in Infants With Orofacial Clefts—A Longitudinal Population-Based Retrospective Radiographic Study of the Primary and Secondary Dentitions

  2021cites this paper
• Orofacial clefts embryology, classification, epidemiology, and genetics.

  2021cites this paper
• Integrative approaches generate insights into the architecture of non-syndromic cleft lip with or without cleft palate

  2021cites this paper
• [Ultrasound scan of a fetus with facial cleft must be done from the lip to the uvula: what's new ?]

  2021cites this paper
• Finger Print, Lip Print and Palatal Print as Genetic Markers in the Inheritance of Non-syndromic Cleft Lip and Palate among Bengali Ethnic Group – A Case-control Study

  2021cites this paper
• Gingival Health Status in Children with And Without Cleft Palate: A Case Control Study

  2020cites this paper
• An integrative, genomic, transcriptomic and network-assisted study to identify genes associated with human cleft lip with or without cleft palate

  2020cites this paper
• From the DEPARTMENT OF DENTAL MEDICINE Karolinska Institutet, Stockholm, Sweden

  2020cites this paper
• Prenatal ultrasound diagnosis of cleft palate without cleft lip, the new ultrasound semiology

  2020cites this paper
• Genetic Factors in Nonsyndromic Orofacial Clefts

  2020cites this paper
• Chemical-Induced Cleft Palate Is Caused and Rescued by Pharmacological Modulation of the Canonical Wnt Signaling Pathway in a Zebrafish Model

  2020cites this paper
• A comprehensive analysis of AHRR gene as a candidate for cleft lip with or without cleft palate.

  2020cites this paper
• Transcriptional analysis of cleft palate in TGFβ3 mutant mice

  2020cites this paper
• Oral mucosal lesions in children with and without cleft lip and palate: a case control study

  2020cites this paper
• SPECC1L regulates palate development downstream of IRF6.

  2020cites this paper
• A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between and maternal smoking, and ANK3

  2019cites this paper
• Likely Pathogenic Variants in One Third of Non-Syndromic Discontinuous Cleft Lip and Palate Patients

  2019cites this paper
• Congenital cleft of the lip and palate in children: pathogenetical significance of matrix metalloproteinases

  2019cites this paper
• WNT10A rs147680216 G>A mutation indicates a higher risk for non-syndromic oral cleft in a northeastern Chinese population.

  2019cites this paper
• TRANSCRIPTOME PROFILING OF CLEFT PALATE IN TGF-3 KNOCKOUT MICE ALLELES : RNA-SEQ ANALYSIS OF TGF-3 MICE By

  2019influential citation
• Polymorphism of reduced folate carrier 1 (A80G) and non-syndromic cleft lip/palate: A systematic review and meta-analysis.

  2019cites this paper
• Implant placement for patients with cleft lip and palate: A clinical report and guidelines for treatment.

  2019cites this paper
• GUIDELINE FOR THE MANAGEMENT OF NAUSEA AND VOMITING IN PREGNANCY AND HYPEREMESIS GRAVIDARUM

  2019cites this paper
• Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports SH3PXD2A as a Clefting Susceptibility Gene

  2019cites this paper
• Exploring the interaction between FGF Genes and T‐box genes among chinese nonsyndromic cleft lip with or without cleft palate case‐parent trios

  2019cites this paper
• p63 establishes epithelial enhancers at critical craniofacial development genes

  2019cites this paper
• A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption

  2019cites this paper
• Trisomy 13 mosaicism syndrome with atypical plurimalformative phenotype

  2019cites this paper
• Unmasking familial CPX by WES and identification of novel clinical signs

  2018cites this paper
• Maternal arsenic exposure and nonsyndromic orofacial clefts.

  2018cites this paper
• Selected Salivary Physicochemical Properties among Cleft Lip and Palate Children in Iraq

  2018cites this paper
• Parental occupational pesticide exposure and nonsyndromic orofacial clefts

  2018cites this paper
• Protein Arginine Methyltransferase PRMT1 Is Essential for Palatogenesis

  2018cites this paper
• A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG

  2018cites this paper
• Creating diversity in mammalian facial morphology: a review of potential developmental mechanisms

  2018cites this paper
• The effects of IRF6 rs2235373 polymorphism on mRNA expression changes in non-syndromic cleft lip and palate with various phenotypes

  2018cites this paper
• A score‐based method for quality control of fetal hard palate assessment during routine second‐trimester ultrasound examination

  2018cites this paper
• There's more to life than perfect plosives: Assessing the psycho-social impact of late intervention for cleft lip/palate using an adapted scale of the Therapy Outcome Measure (TOM)

  2018cites this paper
• Targeting YOD1 by RNA Interference Inhibits Proliferation and Migration of Human Oral Keratinocytes through Transforming Growth Factor-β3 Signaling Pathway

  2018cites this paper
• Analysis of Parent-of-Origin Effects on the X Chromosome in Asian and European Orofacial Cleft Triads Identifies Associations with DMD, FGF13, EGFL6, and Additional Loci at Xp22.2

  2018cites this paper
• Association of the WNT3 polymorphisms and non-syndromic cleft lip with or without cleft palate: evidence from a meta-analysis

  2018cites this paper
• Subphenotyping and Classification of Cleft Lip and Alveolus in Adult Unoperated Patients

  2018cites this paper
• Characterization of deletions in a cohort with cleft lip and palate

  2017cites this paper
• Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects

  2017cites this paper
• TGFß3 / SfaN1 gene variant and the risk factor of nonsyndromic cleft palate only among Indonesian patients.

  2017cites this paper
• A Study on Environmental Factors for Nonsyndromic Cleft Lip and/or Palate

  2017cites this paper
• Evidence for SNP‐SNP interaction identified through targeted sequencing of cleft case‐parent trios

  2017cites this paper
• Transcriptome Profiling of Cleft Palate inTGF-beta3 Knockout Mice Alleles: RNA-SEQ Analysis of TGF-beta3 Mice

  2017influential citation
• Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only

  2017cites this paper
• Massively Increased Caries Susceptibility in an Irf6 Cleft Lip/Palate Model

  2017cites this paper
• Cleft Lip Case in a Middle Bronze Age Young Man from Altai, Russia

  2017cites this paper
• Thyroid cancer causal gene FOXE 1 involved in orofacial clefts in Western Han Chinese

  2017cites this paper
• Genome-wide analysis of parent-of-origin interaction effects with environmental exposure (PoOxE): An application to European and Asian cleft palate trios

  2017cites this paper
• Congenital anomalies associated with syndromic and non-syndromic cleft lip and palate

  2017cites this paper
• Maternal Diabetes, Related Biomarkers and Genes, and Risk of Orofacial Clefts

  2017cites this paper
• Enxertos ósseos alveolares na fissura labiopalatina: protocolos atuais e perspectivas futuras

  2017influential citation
• Association between the IRF6 rs2235371 polymorphism and the risk of nonsyndromic cleft lip with or without cleft palate in Chinese Han populations: A meta-analysis.

  2017cites this paper
• A Review of Systemic Corticosteroid Use in Pregnancy and the Risk of Select Pregnancy and Birth Outcomes.

  2017influential citation
• Genetic analysis of non-syndromic familial multiple supernumerary premolars

  2017cites this paper
• FUNCTIONAL MORPHOLOGY OF TISSUES IN ONTOGENETIC ASPECT IN CHILDREN WITH COMPLETE BILATERAL CLEFT LIP AND PALATE

  2016cites this paper
• Smad2 overexpression rescues the tgf-β3 null mutant mice cleft palate by increased apoptosis

  2016cites this paper
• Mesenchymal Remodeling during Palatal Shelf Elevation Revealed by Extracellular Matrix and F-Actin Expression Patterns

  2016cites this paper
• IRF6 Sequencing in Interrupted Clefting

  2016cites this paper
• Genetic Evaluation for Craniofacial Conditions.

  2016cites this paper
• Using frogs faces to dissect the mechanisms underlying human orofacial defects.

  2016cites this paper
• Salivary Gland and Tooth Abnormalities Massively Increase Caries Susceptibility in A Mouse Model of Cleft Lip/Palate

  2016influential citation
• Expresión Génica del Factor de Crecimiento Transformante Beta en Niños con Fisura Labio Palatina no Sindrómica

  2016cites this paper
• Dental Anomalies in a Brazilian Cleft Population

  2016cites this paper