Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetuses.

Mosca, A L; Pinson, L; Andrieux, J; Copin, H; Bigi, N; Puechberty, J; Sarda, P; Receveur, A; Sevestre, H; Pigeonnat, S; Marle, N; Payet, M; Ragon, C; Rousseau, T; Thauvin-Robinet, C; Masurel-Paulet, A; Schneider, A; Laurent, N; Sagot, P; Mugneret, F; Lefort, G; Faivre, L; Callier, P

Mosca, A L; Pinson, L; Andrieux, J; Copin, H; Bigi, N; Puechberty, J; Sarda, P; Receveur, A; Sevestre, H; Pigeonnat, S; Marle, N; Payet, M; Ragon, C; Rousseau, T; Thauvin-Robinet, C; Masurel-Paulet, A; Schneider, A; Laurent, N; Sagot, P; Mugneret, F; Lefort, G; Faivre, L; Callier, P.

Prenat Diagn ; 31(9): 912-4, 2011 Sep.

Article in En | MEDLINE | ID: mdl-21706508

Subject(s)

Abnormalities, Multiple/genetics; Chromosomes, Human, Pair 15/genetics; Hernias, Diaphragmatic, Congenital; Fetus/abnormalities; Fetus/chemistry; Gene Deletion; Hernia, Diaphragmatic/embryology; Hernia, Diaphragmatic/genetics; Humans

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 15 / Hernias, Diaphragmatic, Congenital Limits: Humans Language: En Journal: Prenat Diagn Year: 2011 Document type: Article

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