Detection of aberrant dna methylation in unique prader - willi syndrome patients and its diagnostic implications

Human Molecular Genetics

Volumn 3, Issue 6, 1994, Pages 893-895

  Buiting, Karin ^a   Dittrich, Bärbel ^a   Robinson, Wendy P ^a,b   Guitart, Mirlam ^a,c   Abeliovich, Dvorah ^a,d   Lerer, Israela ^a,d   Horsthemke, Bernhard ^a  

^a UNIVERSITY HOSPITAL ESSEN   (Germany)

^b Inst für Medizinische Genetik   (Switzerland)

^c HOSPITAL DE SABADELL   (Spain)

^d HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

SMALL NUCLEAR RIBONUCLEOPROTEIN;

ADULT; ARTICLE; CASE REPORT; CHILD; DISOMY; DNA METHYLATION; DNA SEQUENCE; GENE; GENE LOCUS; GENE MUTATION; HUMAN; MALE; PRADER WILLI SYNDROME; PRIORITY JOURNAL;

ADOLESCENT; AUTOANTIGENS; BLOTTING, SOUTHERN; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 15; DNA; DNA, SATELLITE; FEMALE; GENOTYPE; HUMANS; MALE; METHYLATION; PRADER-WILLI SYNDROME; RIBONUCLEOPROTEINS, SMALL NUCLEAR;

EID: 0028343218     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/3.6.893     Document Type: Article

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