Detection of imprinting mutations in Angelman syndrome using a probe for exon alpha of SNRPN.

American journal of medical genetics

Volumn 63, Issue 2, 1996, Pages 414-415

  Beuten, J ^a   Sutcliffe, J S ^a   Casey, B M ^a   Beaudet, A L ^a   Hennekam, R C ^a   Willems, P J ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

AUTOANTIGEN; SM NUCLEAR ANTIGENS; SMALL NUCLEAR RIBONUCLEOPROTEIN;

CPG ISLAND; DNA METHYLATION; DNA PROBE; EXON; GENETICS; GENOME IMPRINTING; HAPPY PUPPET SYNDROME; HUMAN; LETTER; MUTATION; PRADER WILLI SYNDROME; SOUTHERN BLOTTING;

ANGELMAN SYNDROME; AUTOANTIGENS; BLOTTING, SOUTHERN; CPG ISLANDS; DNA METHYLATION; DNA PROBES; EXONS; GENOMIC IMPRINTING; HUMANS; MUTATION; PRADER-WILLI SYNDROME; RIBONUCLEOPROTEINS, SMALL NUCLEAR;

EID: 0030591280     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320630206     Document Type: Letter

References (0)