Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene-Reference-Cited by-同舟云学术

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Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene

Published:2004-02-01 Issue:2 Volume:41 Page:15e-15
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Ghassibe M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 48 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?;American Journal of Medical Genetics Part A;2023-06-23

2. Orthopedic Surgical Management of Complicated Congenital Popliteal Pterygium Syndrome: A Case Report;Orthopedic Research and Reviews;2023-03

3. Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?;2023-02-07

4. Van Der Woude syndrome: A case series at Chu D’ Treichville, Abidjan, Cote D’ Ivoire;Journal of West African College of Surgeons;2023

5. Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder;Italian Journal of Pediatrics;2022-07-29

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