Location of gene for Gorlin syndrome

The Lancet

Volumn 339, Issue 8793, 1992, Pages 581-582

  Farndon, P A ^a   Del Mastro, R G ^a   Kilpatrick, M W ^a   Evans, D R G ^b  

^a UNIVERSITY OF BIRMINGHAM   (United Kingdom)

^b ST MARY S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BASAL CELL CARCINOMA; BASAL CELL NEVUS SYNDROME; CANCER RISK; CARCINOGENESIS; CONTROLLED STUDY; FAMILY STUDY; FEMALE; GENE LOCATION; GENETIC LINKAGE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RISK ASSESSMENT;

BASAL CELL NEVUS SYNDROME; CHROMOSOMES, HUMAN, PAIR 9; GENETIC MARKERS; HAPLOTYPES; HUMAN; LINKAGE (GENETICS); POLYMORPHISM (GENETICS); SUPPORT, NON-U.S. GOV'T;

EID: 0026602737     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/0140-6736(92)90868-4     Document Type: Article

References (8)

1. Nevoid basal cell carcinoma syndrome
2. The incidence of Gorlin syndrome in 173 consecutive cases of medulloblastoma
3. The nevoid basal cell carcinoma syndrome
4. The natural history of the Gorlin (nevoid basal cell carcinoma) syndrome
5. Linkage analysis of the nevoid basal cell carcinoma syndrome. Human Gene Mapping 11 (1991)
6. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
7. Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies