Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding
Author:
Publisher
S. Karger AG
Subject
Genetics(clinical),Genetics,Molecular Biology
Reference10 articles.
1. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements
2. Duplication Dup(1)(q32q44) Detected by Comparative Genomic Hybridization (CGH): Further Delineation of Trisomies 1q
3. Inv dup del (1)(pter?q44::q44?q42:) with the classical phenotype of trisomy 1q42-qter
4. Tandem dup(1p) within the short arm of chromosome 1 in a child with ambiguous genitalia and multiple congenital anomalies
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1. Proteinuric glomerulopathy in an adolescent with a distal partial trisomy chromosome 1;CEN Case Reports;2018-05-16
2. Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings;Molecular Cytogenetics;2018-04-04
3. Opposite chromosome constitutions due to a familial translocation t(1;21)(q43;q22) in 2 cousins with development delay and congenital anomalies;Medicine;2017-04
4. A rare occurrence of two large de novo duplications on 1q42-q44 and 9q21.12-q21.33;Gene;2016-12
5. Partial 1q Duplications and Associated Phenotype;Molecular Syndromology;2015
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