Inherited interstitial 16q21 deletion of 5.8 Mb without apparent phenotypic effect in three generations of a family: An array-CGH study
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference19 articles.
1. Directly transmitted unbalanced chromosome abnormalities and euchromatic variants;Barber;J Med Genet,2005
2. Bilateral frontoparietal polymicrogyria (BFPP) syndrome secondary to a 16q12.1-q21 chromosome deletion involving GPR56 gene;Borgatti;Clin Genet,2009
3. Chromosome imbalance, normal phenotype, and imprinting;Bortotto;J Med Genet,1990
4. A chromosomal deletion map of human malformations;Brewer;Am J Hum Genet,1998
5. High resolution mapping of interstitial long arm deletions of chromosome 16: Relationship to phenotype;Callen;J Med Genet,1993
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Pure 16q21q22.1 deletion in a complex rearrangement possibly caused by a chromothripsis event;Molecular Cytogenetics;2013-08-01
2. Array-CGH revealed one of the smallest 16q21q22.1 microdeletions in a female patient with psychomotor retardation;European Journal of Paediatric Neurology;2013-05
3. A familial deletion of 16q21 characterized by an SNP array and associated with a normal phenotype;American Journal of Medical Genetics Part A;2013-04-30
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