Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

Nature Genetics

Volumn 15, Issue 1, 1997, Pages 87-90

  Hemminki, Akseli ^a   Tomlinson, Ian ^b   Markie, David ^c   Järvinen, Heikki ^d   Sistonen, Pertti ^e   Björkqvist, Anna Maria ^a   Knuutila, Sakari ^a   Salovaara, Reijo ^a   Bodmer, Walter ^b   Shibata, Darryl ^f   De La Chapelle, Albert ^a   Aaltonen, Lauri A ^a  

^a UNIVERSITY OF HELSINKI   (Finland)

^b IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

^c UNIVERSITY OF OTAGO   (New Zealand)

^d UNIVERSITY OF HELSINKI   (Finland)

^e FINNISH RED CROSS BLOOD SERVICE   (Finland)

^f UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 19P; GENE LOCATION; GENE LOCUS; GENETIC LINKAGE; HAMARTOMA; HUMAN; HUMAN TISSUE; HYBRIDIZATION; KARYOTYPE; MALE; PEUTZ JEGHERS SYNDROME; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ADENOCARCINOMA; ADULT; CHROMOSOMES, HUMAN, PAIR 19; FEMALE; GENE DELETION; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMANS; KARYOTYPING; LINKAGE (GENETICS); MALE; NUCLEIC ACID HYBRIDIZATION; PEUTZ-JEGHERS SYNDROME;

EID: 0031012344     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0197-87     Document Type: Article

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