DATABASE: MEDLINE                       LIMITED TO:
SEARCH: su:prader-willi and (genome or genomic) FOUND 59 Records
 
 ____NO.__TITLE_________________________________________AUTHOR___________YEAR
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|     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)
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|   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