Mosaic trisomy of a small r(1) with an abnormal phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference18 articles.
1. Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.
2. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization
3. FISH and molecular studies of autosomal supernumerary marker chromosomes excluding those derived from chromosome 15: II. Review of the literature
4. FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases
Cited by 9 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. Mosaic supernumerary ring chromosome 1 in a three-generational family: 10-year follow-up report;European Journal of Medical Genetics;2011-03
2. Five cases of supernumerary small ring chromosomes 1: Heterogeneity and genotype–phenotype correlation;European Journal of Medical Genetics;2007-03
3. Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation;Cytogenetic and Genome Research;2005-11-03
4. Three new cases with a supernumerary ring chromosome 1;Clinical Dysmorphology;2005-10
5. Supernumerary der(1) marker chromosome derived from a ring chromosome 1 which has retained the original centromere and euchromatin from 1q21.1 ? q21.3 with substantial loss of 1q12 heterochromatin in a female with dysmorphic features and psychomotoric developmental delay;American Journal of Medical Genetics Part A;2005
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