Genotype/phenotype correlation in a patient with partial monosomy 15 and partial trisomy 14
Author:
Publisher
S. Karger AG
Subject
Genetics (clinical),Genetics,Molecular Biology
Reference16 articles.
1. 3:1 Meiotic disjunction in a mother with a balanced translocation, 46,XX,t(5,14)(p15;q13) resulting in tertiary trisomy and tertiary monosomy offspring
2. Chromosome Breakage in the Prader-Willi and Angelman Syndromes Involves Recombination between Large, Transcribed Repeats at Proximal and Distal Breakpoints
3. Case of partial trisomy 9p and partial trisomy 14q resulting from a maternal translocation: Overlapping manifestations of characteristic phenotypes
4. Organisation of the pericentromeric region of chromosome 15: at least four partial gene copies are amplified in patients with a proximal duplication of 15q
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. Somatic 15q Break After Long-Term Stable Disease in Acute Myeloid Leukemia;Clinical Lymphoma Myeloma and Leukemia;2014-04
2. Phenotypic overlapping of trisomy 12p and Pallister–Killian syndrome;European Journal of Medical Genetics;2010-05
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