Pedigree and Genetic Study of a Bilateral Congenital Microtia Family

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Plastic and Reconstructive Surgery

• Publication date

  2010-03-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1097/PRS.0b013e3181ccdbbaPMID 20195123
• 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.

• Environmental and Genetic Factors Associated with Congenital Microtia: A Case-Control Study in Jiangsu, China, 2004 to 2007

  2009cited by this paper
• Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3)

  2009cited by this paper
• In utero exposure to mycophenolate mofetil: A characteristic phenotype?

  2008cited by this paper
• Homozygous FGF3 mutations result in congenital deafness with inner ear agenesis, microtia, and microdontia

  2008cited by this paper
• A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.

  2008cited by this paper
• Cooperative Function of Tbx1 and Brn4 in the Periotic Mesenchyme is Necessary for Cochlea Formation

  2008cited by this paper
• Microtia in Finland: comparison of characteristics in different populations.

  2007cited by this paper
• Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.

  2007cited by this paper
• Molecular changes associated with teratogen-induced cyclopia.

  2007cited by this paper
• Treacher Collins syndrome with a de Novo 5-bp deletion in the TCOF1 gene.

  2006cited by this paper
• Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification.

  2005cited by this paper
• Exclusion of TCOF1 mutations in a case of bilateral Goldenhar syndrome and one familial case of microtia with meatal atresia

  2005cited by this paper
• Epidemiologic characteristics of anotia and microtia in California, 1989-1997.

  2004cited by this paper
• Rates for specific birth defects among native Hawaiians compared to whites, Hawaii 1986-2000.

  2004cited by this paper
• Clinical features, treatment and genetic background of Treacher Collins syndrome.

  2002cited by this paper
• Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome

  2001cited by this paper
• Congenital malformations in Shimla

  2000cited by this paper
• Laterality patterns in infants with external birth defects.

  1999cited by this paper
• Trisomies 13 and 18: Prenatal Diagnosis and Epidemiologic Studies in Hawaii, 1986-1997

  1999cited by this paper
• Microtia: a clinical and genetic study at the National Institute of Pediatrics in Mexico City.

  1999cited by this paper
• Altitude as a risk factor for congenital anomalies.

  1999cited by this paper
• Heterogeneous rates for birth defects in Latin America: Hints on causality

  1996cited by this paper
• The epidemiology of anotia and microtia.

  1996cited by this paper
• Epidemiology and genetics of microtia-anotia: a registry based study on over one million births.

  1995cited by this paper
• Achondrogenesis type II with polydactyly.

  1995cited by this paper
• BMP5 and the molecular, skeletal, and soft-tissue alterations in short ear mice.

  1994cited by this paper
• The association of facial palsy and/or sensorineural hearing loss in patients with hemifacial microsomia.

  1989cited by this paper
• Prevalence rates of microtia in South America.

  1986cited by this paper
• Plastic and reconstructive surgery

  1978cited by this paper
• Data Collection Methods: Review of existing data systems.

  year unknowncited by this paper

• Genetics of Nonsyndromic Microtia and Congenital Aural Atresia: A Scoping Review.

  2024cites this paper
• Differential Expression of Noncoding RNAs Revealed Enhancer RNA AC016735.2 as a Potential Pathogenic Marker of Congenital Microtia Patients

  2024cites this paper
• Genetics and Epigenetics in the Genesis and Development of Microtia

  2024cites this paper
• The circular RNA expression profile of human auricle cartilage and the role of circCOL1A2 in isolated microtia.

  2023cites this paper
• The role of genetic factors in microtia: A systematic review

  2022cites this paper
• The role of genetic factors in microtia: A systematic review [version 2; peer review: 1 approved with reservations, 1 not approved]

  2022cites this paper
• The role of genetic factors in microtia: A systematic review [version 1; peer review: awaiting peer review]

  2022cites this paper
• Key Genes Identified in Nonsyndromic Microtia by the Analysis of Transcriptomics and Proteomics

  2022cites this paper
• Congenital Anomalies of The Ear in Newborns from Lviv Region (west Ukraine) for 2006-2018 YY.

  2020cites this paper
• Genetic Advances in the Understanding of Microtia

  2016cites this paper
• Congenital Auricular Malformations: Description of Anomalies and Syndromes

  2015cites this paper
• [Microtia-atresia: clinical, genetic and genomic aspects].

  2014cites this paper
• The genetics of auricular development and malformation: new findings in model systems driving future directions for microtia research.

  2014cites this paper
• Genome-Wide Linkage Study Suggests a Susceptibility Locus for Isolated Bilateral Microtia on 4p15.32–4p16.2

  2014cites this paper
• MicroRNA expression profiling and target genes study in congenital microtia.

  2013cites this paper
• Microtia: Epidemiology and genetics

  2012cites this paper
• SÍNDROME DE TREACHER COLLINS ASOCIADO A MALFORMACIONES AERODIGESTIVAS MÚLTIPLES

  2011cites this paper