DOI:
10.1055/s-00000015
European Journal of Pediatric Surgery
LinksClose Window
References
Jaillard S, Loget P, Lucas J. et al.
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.
Eur J Med Genet 2011;
54 (02) 186-188
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.