FISH analysis in Prader-Willi and Angelman syndrome patients
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference20 articles.
1. (1990): Birth Defects Encyclopedia, Center for Birth Defects Information Services. Dover, MA, Blackwell Scientific Publications, Inc.
2. A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes
3. DNA deletion and its parental origin in Angelman syndrome patients
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1. A Comprehensive Review of Genetically Engineered Mouse Models for Prader-Willi Syndrome Research;International Journal of Molecular Sciences;2021-03-31
2. Identification of a rare de novo three-way complex t(5;20;8)(q31;p11.2;p21) with microdeletions on 5q31.2, 5q31.3, and 8p23.2 in a patient with hearing loss and global developmental delay: case report;Molecular Cytogenetics;2009-01-07
3. Analysis of the Prader-Willi syndrome chromosome region using quantitative microsphere hybridization (QMH) array;American Journal of Medical Genetics Part A;2008-09-15
4. Molecular characterization of a novel X-linked syndrome involving developmental delay and deafness;American Journal of Medical Genetics Part A;2007
5. Prader–Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15—case report plus review of similar cases;European Journal of Medical Genetics;2005-04
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