Exclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader-Willi syndrome

Human Genetics

Volumn 116, Issue 3, 2005, Pages 228-230

  Runte, Maren ^a,c   Varon, Raymonda ^b   Horn, Denise ^b   Horsthemke, Bernhard ^a   Buiting, Karin ^a  

^a UNIVERSITY HOSPITAL ESSEN   (Germany)

^b HUMBOLDT UNIVERSITY   (Germany)

^c UNIVERSITY OF TÜBINGEN   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

SMALL NUCLEOLAR RNA;

ARTICLE; CENTROMERE; DNA FLANKING REGION; FAMILY STUDY; GENE CLUSTER; GENE DELETION; GENE FUNCTION; GENE LOSS; GENE MAPPING; GENE SEQUENCE; HAPPY PUPPET SYNDROME; HUMAN; MULTIGENE FAMILY; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PHENOTYPE; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RNA STRUCTURE;

FEMALE; GENOMIC IMPRINTING; HUMANS; MALE; MOLECULAR SEQUENCE DATA; PEDIGREE; PRADER-WILLI SYNDROME; RNA, SMALL NUCLEOLAR;

EID: 13144282733     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00439-004-1219-2     Document Type: Article

References (7)

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