Un caso de deleción parcial 1p36.1 y trisomía parcial 6p diagnosticadas por cariotipo
Author:
Publisher
Sociedad Chilena de Pediatria
Subject
Pediatrics, Perinatology and Child Health
Link
https://www.sciencedirect.com/science/article/pii/S0370410616300195/pdfft?isDTMRedir=true&download=true
Reference18 articles.
1. Further delineation of deletion 1p36 syndrome in 60 patients: A recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008
2. Morbid obesity in a child with monosomy 1p36 syndrome;Zagalo;BMJ Case Reports.,2012
3. Multiple causes of apnea in 1p36 deletion syndrome include seizures;Kanabar;SeizureV 21,2012
4. Clinical expression of an inherited unbalanced translocation in chromosome 6;Ganguly;Case Rep Genet,2011
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