Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case
Author:
Affiliation:
1. Department of Medical Genetics; Faculty of Medicine; Gazi University; Besevler Ankara Turkey
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference31 articles.
1. 1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay;Abdelmoity;Eur J Med Genet,2011
2. Duplication or amplification of chromosome band 11q23, including the unrearranged MLL gene, is a recurrent abnormality in therapy-related MDS and AML, and is closely related to mutation of the TP53 gene and to previous therapy with alkylating agents;Andersen;Genes Chromosomes Cancer,2001
3. A familial cryptic subtelomeric deletion 12p with variable phenotypic effect;Baker;Clin Genet,2002
4. Distal 12p deletion in a stillborn infant;Baroncini;Am J Med Genet,1990
Cited by 2 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. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21;Genetics and Molecular Research;2016
2. Clinical and molecular evaluations of siblings with “pure” 11q23.3-qter trisomy or reciprocal monosomy due to a familial translocation t (10;11) (q26;q23.3);Molecular Cytogenetics;2014-12
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