Fine deletion mapping on the long arm of chromosome 9 in sporadic and familial basal cell carcinomas

Human Molecular Genetics

Volumn 4, Issue 1, 1995, Pages 129-133

  M shanley, Susan ^a   Dawkins, Hugh ^a,b   J wainwright, Brandon ^a,c   Wicking, Carol ^a,c   Heenan, Peter ^a,b   Eldon, Michael ^a,b   Searle, Jeffrey ^a,d   Chenevlx trench, Georgia ^a  

^a QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

^b UNIVERSITY OF WESTERN AUSTRALIA   (Australia)

^c UNIVERSITY OF QUEENSLAND   (Australia)

^d ROYAL BRISBANE AND WOMEN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; BASAL CELL CARCINOMA; CANCER SUSCEPTIBILITY; CHROMOSOME 9; CONGENITAL DISORDER; CONTROLLED STUDY; ETIOLOGY; FAMILIAL CANCER; GENE DELETION; GENE LOSS; GENE MAPPING; GENETIC SUSCEPTIBILITY; HUMAN; HUMAN TISSUE; MAJOR CLINICAL STUDY; PRIORITY JOURNAL;

ADULT; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 9; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HUMAN; NEOPLASMS, BASAL CELL; NEVUS; SKIN NEOPLASMS; SUPPORT, NON-U.S. GOV'T; SYNDROME;

EID: 0028801755     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/4.1.129     Document Type: Article

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