Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13

American Journal of Medical Genetics

Volumn 70, Issue 3, 1997, Pages 222-228

  Eliez, Stephan ^a,b   Morris, Michael A ^a   Dahoun Hadorn, Sophie ^a   DeLozier Blanchet, C Dawn ^a   Gos, Arnaud ^a   Sizonenko, Pierre ^a   Antonarakis, Stylianos E ^a  

^a UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^b Division of Medical Genetics   (Switzerland)

Author keywords

Chromosome 15; Microdeletion; Prader Willi syndrome; Translocation; Y chromosome

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHROMOSOME 15Q; CHROMOSOME TRANSLOCATION; CYTOGENETICS; FEMALE; GENE DELETION; GENETIC PREDISPOSITION; HUMAN; HUMAN CELL; HUMAN TISSUE; MEIOSIS; MITOSIS; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

ADOLESCENT; BLOTTING, SOUTHERN; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 15; DNA, SATELLITE; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; KARYOTYPING; PEDIGREE; PRADER-WILLI SYNDROME; TRANSLOCATION, GENETIC; Y CHROMOSOME;

EID: 0030977970     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970613)70:3<222::AID-AJMG3>3.0.CO;2-Y     Document Type: Article

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