DATABASE: MEDLINE LIMITED TO: SEARCH: su:prader-willi and (genome or genomic) FOUND 59 Records ____NO.__TITLE_________________________________________AUTHOR___________YEAR | | 1 Inherited microdeletions in the Angelman ... Buiting K 1995 | 2 The link between cytogenetics and mendelism. Dallapiccola B 1995 | 3 The mouse pink-eyed dilution gene: associ... Brilliant MH 1994 | 4 Diagnosing Prader-Willi syndrome. Young ID 1995 | 5 Tissue-specific and allele-specific repli... Gunaratne PH 1995 | 6 Parental imprinting and the IGF2 gene. Ekstrom TJ 1994 | 7 Impressions of imprints. Ohlsson R 1994 | 8 Inv dup(15) supernumerary marker chromoso... Webb T 1994 | 9 In and around SNRPN news; comment Lalande M 1994 | 10 Deletions of a differentially methylated ... Sutcliffe JS 1994 | 11 Relevance of genomic imprinting to human ... Solter D 1992 | 12 Imprinting analysis of three genes in the... Nakao M 1994 | 13 New insights reveal complex mechanisms in... Nicholls RD 1994 | 14 Prader-Willi syndrome: diagnostic strateg... Malzac P 1993 | 15 The human gamma-aminobutyric acid recepto... Glatt K 1994 | 16 Genomic imprinting: a new mechanism for d... Langlois S 1994 DATABASE: MEDLINE LIMITED TO: SEARCH: su:prader-willi and (genome or genomic) Record 4 of 59__________________________________________(Page 1 of 2) | | RECORD NO.: 95302856 | AUTHOR: Young ID | ADDRESS: Clinical Genetic Service, City Hospital, Nottingham, UK. | TITLE: Diagnosing Prader-Willi syndrome. | SOURCE: Lancet (L0S), 1995 Jun 24; 345 (8965): 1590 | LANGUAGE: English | COUNTRY PUB.: ENGLAND | ANNOUNCEMENT: 9509 | PUB. TYPE: JOURNAL ARTICLE |MESH HEADINGS: Prader-Willi Syndrome--diagnosis (*DI)/genetics (*GE); | Chromosome Deletion; Chromosomes, Human, Pair 15--genetics | (GE); DNA--analysis (AN); DNA Probes; Genomic Imprinting; In | Situ Hybridization, Fluorescence; Methylation; Human | GENE SYMBOL: SNRPN |CHEMICAL SUBS: 0 (DNA Probes); 9007-49-2 (DNA) | STANDARD NO.: 0140-6736 | DATES: Entered 950717