Author:
France H. F. de,Beemer F. A.,Ippel P. F.
Subject
Genetics (clinical),Genetics
Reference12 articles.
1. Prader Willi syndrome: Are there population differences;Butler;Clin. Genet.,1982
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3. Trisomie 15 partielle, 47, XY,+del(15)(q21);Echenne;Pediatric T,1981
4. Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment;Fraccaro;Hum. Genet.,1983
5. Congenital heart disease with del(15q) mosaicism;Herva;Clin. Genet.,1980
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