A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

BACKGROUND: Copy number variants (CNVs) may play an important part in the development of common birth defects such as oral clefts, and individual patients with multiple birth defects (including clefts) have been shown to carry small and large chromosomal deletions. In this paper we investigate de no...

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Detalles Bibliográficos
Autores principales: Younkin, Samuel G, Scharpf, Robert B, Schwender, Holger, Parker, Margaret M, Scott, Alan F, Marazita, Mary L, Beaty, Terri H, Ruczinski, Ingo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929298/
https://www.ncbi.nlm.nih.gov/pubmed/24528994
http://dx.doi.org/10.1186/1471-2156-15-24

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929298/
https://www.ncbi.nlm.nih.gov/pubmed/24528994
http://dx.doi.org/10.1186/1471-2156-15-24

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