Narrowing the deleted region associated with the 15q21 syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference14 articles.
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3. Craniosynostosis in an infant with an interstitial deletion of 15q [46,XY,del(15)(q15q22.1)];Fukushima;Am. J. Med. Genet.,1990
4. The complex nature of constitutional de novo apparently balanced translocations in patients presenting with abnormal phenotypes;Gribble;J. Med. Genet.,2005
5. Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q;Gunn;Am. J. Med. Genet. A.,2003
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1. De novointerstitial deletion of 15q22q23 with global developmental delay and hypotonia: the first Korean case;Korean Journal of Pediatrics;2015
2. Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA;European Journal of Medical Genetics;2014-03
3. Clinical and Molecular Characterization of a Patient with 15q21.2q22.2 Deletion Syndrome;Cytogenetic and Genome Research;2014
4. First reported case of interstitial 15 q15.3-q21.3 deletion diagnosed prenatally and characterized with array CGH in a fetus with an isolated short femur;American Journal of Medical Genetics Part A;2012-02-02
5. Knockout of G protein β5 impairs brain development and causes multiple neurologic abnormalities in mice;Journal of Neurochemistry;2011-09-23
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