Genetic studies in congenital anterior midline cervical cleft
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference14 articles.
1. A human homologue of the Drosophila eyes absent gene underlies branchio-oto-renal (BOR) syndrome and identifies a novel gene family;Abdelhak;Nat Genet,1997
2. Mutation of the gene encoding human TTF-2 associated with thyroid agenesis, cleft palate and choanal atresia;Clifton-Bligh;Nat Genet,1998
3. Identification of the gene for oral-facial-digital type I syndrome;Ferrante;Am J Hum Genet,2001
4. Genetic aspects of the BOR syndrome-branchial fistulas, ear pits, hearing loss, and renal anomalies;Fraser;Am J Med Genet,1978
5. Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome;Hoskins;Am J Hum Genet,2007
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1. Congenital midline cervical cleft: Management of a case series and literature review;Journal of Plastic, Reconstructive & Aesthetic Surgery;2024-06
2. A delayed diagnosis of congenital midline cervical cleft;Clinical Case Reports;2022-03
3. Congenital Midline Cervical Cleft: A Variant of Tessier Number 30 Cleft Causing Micrognathia;The Cleft Palate-Craniofacial Journal;2021-01-13
4. Congenital midline cervical cleft: An easily misdiagnosed disease;Archives of Craniofacial Surgery;2020-12-20
5. Congenital Midline Cervical Cleft: First Report and Genetic Analysis of Two Related Patients;Annals of Otology, Rhinology & Laryngology;2020-02-06
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