Phenotypic variation in two patients with a ring chromosome 22
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1979.tb01007.x/fullpdf
Reference23 articles.
1. A case of ring chromosome G22;Brookfield;J. med. Genet.,1976
2. G-deletion syndrome II;Chauvel;Hum. Genet.,1972
3. Identification of 21r and 22r chromosomes by quinacrine fluorescence;Crandall;Clin. Genet.,1972
4. Indications for chromosome analysis illustrated by a case of ring 22;Howard-Peebles;J. Hered.,1977
5. Phenotypic correlations in patients with ring chromosome 22;Hunter;Clin. Genet.,1977
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2. Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion;American Journal of Medical Genetics Part A;2014-04-03
3. Ring Chromosome 22: A Review of the Literature and First Report from India;Balkan Journal of Medical Genetics;2012-01-01
4. The use of sequential silver and quinacrine staining to determine the parental origin and breakpoints of a ring-22 human chromosome;Clinical Genetics;2008-04-23
5. An investigation into sub-telomeric deletions of chromosome 22 and pervasive developmental disorders;American Journal of Medical Genetics;2004
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