Linkage and LOH studies in 19 cylindromatosis families show no evidence of genetic heterogeneity and refine the CYLD locus on chromosome 16q12-q13

Human Genetics

Volumn 106, Issue 1, 2000, Pages 58-65

  Takahashi, Meiko ^a   Rapley, Elizabeth ^a   Biggs, Patrick J ^a,r   Lakhani, Sunil R ^b   Cooke, David ^s   Hansen, Juliana ^c   Blair, Edward ^d   Hofmann, B ^e   Siebert, Reiner ^f   Turner, Gwen ^g   Evans, D Gareth ^h   Schrander Stumpel, Connie ⁱ   Beemer, Frits A ^j   Van Vloten, Willem A ^j   Breuning, Martijn H ^k   Van Den Ouweland, Ans ^l   Halley, Dicky ^l   Delpech, Bertrand ^m   Cleveland, Mark ⁿ   Leigh, Irene ^o   Chapman, Pam ^p   Burn, John ^p   Hohl, Daniel ^q   Görög, Jean Philippe ^q   Seal, Sheila ^a   Mangion, Jon ^a   Warren, William ^a   Bignell, Graham ^a   Stratton, Michael R ^a   more..

^a INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^b ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^d OXFORD UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^e HEINRICH HEINE UNIVERSITY   (Germany)

^f UNIVERSITY OF KIEL   (Germany)

^g Department of Clinical Genetics ^*  (United Kingdom)

^h ST MARY S HOSPITAL   (United Kingdom)

ⁱ MAASTRICHT UNIVERSITY MEDICAL CENTER   (Netherlands)

^j UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^k LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

^l ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^m CENTRE HENRI BECQUEREL   (France)

ⁿ UNIVERSITY OF IOWA   (United States)

^o ST BARTHOLOMEW S HOSPITAL   (United Kingdom)

^p NEWCASTLE UNIVERSITY   (United Kingdom)

^q LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^r BAYLOR COLLEGE OF MEDICINE   (United States)

^s Maryborough Hospital   (Australia)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CANCER SUSCEPTIBILITY; CHROMOSOME 16Q; CHROMOSOME MAP; CONTROLLED STUDY; CYLINDROMA; FEMALE; GENE FREQUENCY; GENE LOCUS; GENE MAPPING; GENETIC HETEROGENEITY; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; ONCOGENE; PRIORITY JOURNAL; SKIN TUMOR; TUMOR SUPPRESSOR GENE;

CARCINOMA, ADENOID CYSTIC; CHROMOSOMES, HUMAN, PAIR 16; FEMALE; GENETIC HETEROGENEITY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); LOD SCORE; LOSS OF HETEROZYGOSITY; MALE; MICROSATELLITE REPEATS; PEDIGREE; POLYMORPHISM, GENETIC; SKIN NEOPLASMS; SYNDROME;

EID: 0034017283     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004399900227     Document Type: Article

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