A high-resolution radiation hybrid map of the region surrounding the Gorlin syndrome gene

European Journal of Human Genetics

Volumn 4, Issue 4, 1996, Pages 242-245

  Obermayr, Franz ^a  

^a IMPERIAL CANCER RESEARCH FUND   (United Kingdom)

Author keywords

24 markers; ESTs; Gorlin syndrome; Radiation hybrid map; RHMAP; XPA

Indexed keywords

ARTICLE; BASAL CELL CARCINOMA; BASAL CELL NEVUS SYNDROME; CELL FUSION; CHROMOSOME 9Q; CONTROLLED STUDY; DISEASE PREDISPOSITION; GENE DELETION; GENE MAPPING; HUMAN; HUMAN CELL; HYBRID CELL; IRRADIATION; MARKER GENE; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; YEAST ARTIFICIAL CHROMOSOME;

CRICETINAE;

EID: 0029814926     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472206     Document Type: Article

References (2)

1. Gailani MR, Bale SJ, Leffell DJ, diGiovanna JJ, Peck GL, Poliak S, Drum MA, Patakia B, McBride OW, Kase R, Greene M, Mulvihill JJ, Bale AE: Developmental defects in Gorlin syndrome related to a putative tumor suppressor gene on chromosome 9. Cell 1992;69:111-117.
2. Farndon PA, Del MR, Evans DG, Kilpatrick MW: Location of gene for Gorlin syndrome. Lancet 1992;339:581-582.