Molecular diagnosis of Prader-Willi syndrome: comparison of cytogenetic and molecular genetic data including parent of origin dependent methylation DNA patterns.

American journal of medical genetics

Volumn 61, Issue 2, 1996, Pages 188-190

  Butler, M G ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ADOLESCENT; ADULT; CHEMISTRY; CHILD; CHROMOSOME 15; CHROMOSOME ABERRATION; DNA PROBE; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENETICS; HUMAN; INFANT; KARYOTYPING; LETTER; MALE; METHYLATION; POLYMERASE CHAIN REACTION; PRADER WILLI SYNDROME; PRESCHOOL CHILD; SOUTHERN BLOTTING;

ADOLESCENT; ADULT; BLOTTING, SOUTHERN; CHILD; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 15; DNA; DNA PROBES; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; KARYOTYPING; MALE; METHYLATION; POLYMERASE CHAIN REACTION; PRADER-WILLI SYNDROME; SEQUENCE DELETION;

EID: 0030579609     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320610202     Document Type: Letter

References (0)