Case report of an extra, small, acrocentric chromosome in a non-mongoloid girl
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1974.tb01691.x/fullpdf
Reference8 articles.
1. Additional G-like chromosome in a malformed boy;Fraccaro;J. med. Genet.,1971
2. Three non-mongoloid patients of similar phenotype with an extra G- like chromosome;Gustavsson;Clin. Genet.,1972
3. Mongolism and other abnormalities in a family with trisomy 21-22 tendency;Hall;Acta paediat. (Uppsala),1963
4. Trisomy 22: A clinical entity;Hsu;J. Pedint.,1971
5. Partielle Trisomie D1 - eine seltene Chro-mosomanomalie;Krüger;Hum. Genet.,1968
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1. INTERCHROMOSOMAL DUPLICATION FOR THE SHORT ARM OF CHROMOSOME No. 9: REPORT OF THREE CASES DUE TO A FAMILIAL TRANSLOCATION t(9; 11) AND ONE CASE WITH A DE NOVO 47, XX, + 9p KARYOTYPE;Journal of Intellectual Disability Research;2008-06-28
2. Trisomy 9 (pter → q1 to q3): the phenotype as an objective aid to karyotypic interpretation;Clinical Genetics;2008-04-23
3. Trisomy 9p with an isochromosome of 9p;Human Genetics;1979
4. Genetics of the +p9 syndrome;Human Genetics;1976
5. A new contribution to the study of 22 trisomy;Humangenetik;1975
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