TY  - GEN
AU  - Jaillard,Sylvie
AU  - Loget,Philippe
AU  - Lucas,Josette
AU  - Dubourg,Christèle
AU  - Le Bouar,Gwenaelle
AU  - Demurger,Florence
AU  - Bertorello,Isabelle
AU  - David,Véronique
AU  - Poulain,Patrice
AU  - Odent,Sylvie
AU  - Belaud-Rotureau,Marc-Antoine
TI  - Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect
SN  - 1878-0849
PY  - 2011///0804
KW  - Chromosome Deletion
KW  - Chromosome Inversion
KW  - Chromosomes, Human, Pair 15
KW  - Chromosomes, Human, X
KW  - Female
KW  - Heart Defects, Congenital
KW  - genetics
KW  - Hernia, Diaphragmatic
KW  - Hernias, Diaphragmatic, Congenital
KW  - Humans
KW  - Infant, Newborn
KW  - X Chromosome Inactivation
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1016/j.ejmg.2010.11.001
ER  -