Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2→q25.3)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb00462.x/fullpdf
Reference18 articles.
1. A case of inverted insertion assessed by R and G banding;Arce;J. Med. Genet.,1982
2. Nouveau système de marquage chromosomique. Les bandes T;Dutrillaux;Chromosoma (Berlin),1973
3. Partial proximal trisomy of the long arm of chromosome 5 (q13q22) resulting from maternal insertion der ins (10;5);Gilgenkrantz;J. Med. Genet.,1981
4. Familial insertional translocation;Grace;Lancet,1972
5. An interstitial translocation: chromosome no. 1p to 4q;Gray;Lancet,1972
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1. Proximal duplication of the long arm of chromosome 10 (10q11.2 → 10q22): a distinct clinical entity;Clinical Genetics;2008-06-28
2. Congenital cardiovascular malformations (CCVM) and structural chromosome abnormalities: a report of 9 cases and literature review;Clinical Genetics;2008-06-28
3. Adult with an interstitial deletion of chromosome 10 [del(10)(q25.1q25.3)]: Overlap with Coffin-Lowry Syndrome;American Journal of Medical Genetics;2000
4. Partial monosomy of distal 10q: Three new cases and a review;American Journal of Medical Genetics;1999-09-03
5. Segregation of a familial balanced (12;10) insertion resulting in dup(10)(q21.2q22.1) and del(10)(q21.2q22.1) in first cousins;American Journal of Medical Genetics;1997-03-17
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