Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference29 articles.
1. Partial trisomy of the long arm of chromosome 1 due to a familial translocation t(1;10)(q32;q26)
2. Trisomy (1q) (q42→qter): confirmation of a syndrome
3. Congenital Ocular Defects Associated With an Abnormality of the Human Chromosome 1: Trisomy 1q32-qter
4. Partial trisomy 1(q42-->qter): a new case with a mild phenotype.
5. Detection of a de novo duplication of 1q32-qter by fluorescence in situ hybridisation in a boy with multiple malformations: further delineation of the trisomy 1q syndrome.
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1. Partial 1q Duplications and Associated Phenotype;Molecular Syndromology;2015
2. Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes;BMC Medical Genomics;2014-09-15
3. Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up;Molecular Cytogenetics;2014-08-22
4. Partial trisomy 1q41-qter and partial trisomy 9pter-9q21.32 in a newborn infant: An array CGH analysis and review;American Journal of Medical Genetics Part A;2013-12-05
5. 1q44-qter Trisomy:Clinical Report and Review of the Literature;Genetic Testing and Molecular Biomarkers;2009-02
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