Developmental defects in gorlin syndrome related to a putative tumor suppressor gene on chromosome 9

Cell

Volumn 69, Issue 1, 1992, Pages 111-117

  Gailani, Mae R ^a   Bale, Sherri J ^b   Leffell, David J ^a   DiGiovanna, John J ^b   Peck, Gary L ^b   Poliak, Susanna ^b   Drum, M Ann ^c   Pastakia, Behram ^d   McBride, O W ^b   Kase, Ronald ^e   Greene, Mark ^b   Mulvihill, John J ^b   Bale, Allen E ^a,e  

^a YALE UNIVERSITY   (United States)

^b NATIONAL CANCER INSTITUTE   (United States)

^c NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^d NATIONAL INSTITUTES OF HEALTH   (United States)

^e WESTAT   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ALLELE; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BASAL CELL CARCINOMA; BASAL CELL NEVUS SYNDROME; CANCER GENETICS; CARCINOGENESIS; CELL GROWTH; CHROMOSOME 9; CHROMOSOME DELETION; CLINICAL ARTICLE; CONGENITAL MALFORMATION; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; GENETIC MARKER; HUMAN; HUMAN CELL; HUMAN TISSUE; MEDULLOBLASTOMA; OVARY TUMOR; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

BASAL CELL NEVUS SYNDROME; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GENES, TUMOR SUPPRESSOR; HETEROZYGOTE; HUMAN; LINKAGE (GENETICS); MALE; MUTATION; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; SUPPORT, NON-U.S. GOV'T;

EID: 0026627965     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/0092-8674(92)90122-S     Document Type: Article

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