Two cases of prenatally diagnosed diaphragmatic hernia accompanied by the same undescribed chromosomal deletion (15q24 de novo)
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1998.tb02706.x/fullpdf
Reference5 articles.
1. Conference report: First International Scientific Workshop on Prader-Willi syndrome and other chromosome 15q deletion disorders;Cassidy;Am J Med Genet,1992
2. An infant with deletion of the distal long arm of chromosome 15 (q26.1-ter) and loss of insulin-like growth factor 1 receptor gene;Roback;Am J Med Genet,1991
3. Insulin-like growth factor 1 receptor expression and function in fibroblasts from two patients with deletion of the distal long arm of chromosome 15;Siebler;J Clin Endocrinol Metab,1995
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2. Genetic Diagnostic Strategies and Counseling for Families Affected by Congenital Diaphragmatic Hernia;European Journal of Pediatric Surgery;2021-12
3. Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping;Human Genetics;2009-06-26
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