Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference11 articles.
1. Intensity heteromorphisms of human chromosome 15p by DA/DAPI technique
2. DA/DAPI heteromorphisms in acrocentric chromosomes other than 15
3. A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.
4. Chromosome 15 anomalies and the Prader-Willi syndrome: Cytogenetic analysis
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1. Electroclinical features of epilepsy in patients with InvDup(15);Seizure;2017-04
2. Clinical review of genetic epileptic encephalopathies;European Journal of Medical Genetics;2012-05
3. The behavioral phenotype of the idic(15) syndrome;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2010-10-27
4. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q);Orphanet Journal of Rare Diseases;2008-11-19
5. Chromosomal disorders associated with epilepsy;Epileptic Disorders;2005-09
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