Deletion of 16q with prolonged survival and unusual radiographic manifestations
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference19 articles.
1. Confirmation of a suspected 16q deletion in a dysmorphic child by flow karyotype analysis.
2. Deletion of the Long Arm of Chromosome 16 and an Unexpected Duffy Blood Group Phenotype reveal a Possible Autosomal Linkage
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1. Deletion of 16q22.2q23.3 in a Boy with a Phenotype Reminiscent of Silver-Russell Syndrome;Molecular Syndromology;2021
2. Oculofacial Manifestations of Chromosomal Aberrations;The Eye in Pediatric Systemic Disease;2017
3. Chromosomes and the Skin;Harper's Textbook of Pediatric Dermatology;2011-05-24
4. Description of the smallest critical region for Dandy-Walker malformation in chromosome 13 in a girl with a cryptic deletion related to t(6;13)(q23;q32);American Journal of Medical Genetics Part A;2010-08-03
5. De novo interstitial deletion 16(q12. 1q13) of paternal origin in a 10-year-old boy;Clinical Genetics;2008-06-28
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