Pattern of cytogenetic abnormalities in syndromic mental retardation/intellectual disability in Kashmir region of Jammu and Kashmir
Author:
Funder
Government of India Department of Biotechnology
Publisher
Elsevier BV
Subject
Genetics
Reference38 articles.
1. Parental origin and timing of de novo robertsonian translocation formation;Bandyopadhyay;Am. J. Hum. Genet.,2002
2. Chromosomal abnormalities in patients with intellectual disability: a 21-year retrospective study;Belkady;Hum. Hered.,2019
3. A patient with down syndrome with a de novo derivative chromosome 21;Cetin;Gene,2012
4. Advances in understanding genetic basis of intellectual disability;Chiurazzi;F1000 Res. Faculty Rev.,2016
5. Molecular mapping of twenty-four features of Down’s syndrome onchromosome 21;Delabar;Eur. J. Hum. Genet.,1993
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