Microdeletion of the entire IRF6 gene in a Subsaharian African’s family with Van der Woude syndrome-Reference-Cited by-同舟云学术

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Microdeletion of the entire IRF6 gene in a Subsaharian African’s family with Van der Woude syndrome

Published:2020-01 Issue:1 Volume:29 Page:24-27
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Mbuyi-Musanzayi Sébastien,Kasamba Eric I.,Revencu Nicole,Lukusa Prosper T.,Kalenga Prosper M.,Tshilombo François K.,Reychler Hervé,Devriendt Koenraad

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Reference25 articles.

1. Lip pits and deletion 1q32––41.;Bocian;Am J Med Genet,1987

2. Genetic analysis in families with Van der Woude syndrome.;Burdick;J Craniofac Genet Dev Biol,1985

3. Novel IRF6 mutations in families with Van der Woude syndrome and popliteal pterygium syndrome from sub-Saharan Africa.;Butali;Mol Genet Genomic Med,2014

4. Familial incidence of labial pits.;Cheney;Am J Otolaryngol,1986

5. Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Brazilian population with high African ancestry.;do Rego Borges;Am J Med Genet A,2015

Cited by 2 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. Identification of copy neutral loss of heterozygosity on chromosomes 1p, 1q, and 6p among nonsyndromic cleft lip and/or without cleft palate with hypodontia;BMC Oral Health;2023-11-29

2. Non‐random distribution of deleterious mutations in the DNA and protein‐binding domains of IRF6 are associated with Van Der Woude syndrome;Molecular Genetics & Genomic Medicine;2020-06-17

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