A boy with proximal trisomy 15 and a male foetus with distal trisomy 15 due to a familial 13p;15q translocation
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb01404.x/fullpdf
Reference11 articles.
1. A G-like trisomy with a major 15-proximal supernumerary component derived from a D/E balanced maternal interchange;Bannister;J. Pediat.,1975
2. Differential binding of alkylating fluochromes in human chromosomes;Caspersson;Exp. Cell Res.,1970
3. Partial trisomy of chromosome number 15 identified by trypsin-giemsa banding;Crandall;Amer. J. ment. Defic.,1973
4. Inherited partial duplication of chromosome no. 15. J;Fujimoto;med. Genet.,1974
5. Leucocytes cultured from small inocula of whole blood and the preparation of metaphase chromosomes by treatment with hypotonic HCI;Hungerford;Stain Technol.,1965
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1. References;Benign & Pathological Chromosomal Imbalances;2014
2. A Girl with 15q Overgrowth Syndrome and dup(15)(q24q26.3) that Included Telomeric Sequences;Annals of Laboratory Medicine;2010-06-01
3. A rare case of trisomy 15pter-q21.2 due to a de novo marker chromosome;American Journal of Medical Genetics Part A;2010-03
4. Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein to 18q22.3;American Journal of Medical Genetics;1996-04-09
5. Trisomy 15 mosaicism in an IVF fetus.;Journal of Medical Genetics;1992-10-01
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