Localization of the gene for Cowden disease to chromosome 10q22-23

Nature Genetics

Volumn 13, Issue 1, 1996, Pages 114-116

  Nelen, M R ^a   Padberg, G W ^a   Peeters, E A J ^b   Lin, A Y ^c   Van Den Helm, B ^a   Frants, R R ^b   Coulon, V ^d   Goldstein, A M ^c   Van Reen, M M M ^a   Easton, D F ^e   Eeles, R A ^f   Hodgson, S ^g   Mulvihill, J J ^h   Murday, V A ⁱ   Tucker, M A ^c   Mariman, E C M ^a   Starink, T M ^j   Ponder, B A J ^k   Ropers, H H ^a   Kremer, H ^a   Longy, M ^d   Eng, C ^k,l   more..

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b LEIDEN UNIVERSITY   (Netherlands)

^c NATIONAL CANCER INSTITUTE   (United States)

^d INSTITUT BERGONIÉ   (France)

^e UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^f ROYAL MARSDEN HOSPITAL   (United Kingdom)

^g GUY'S AND ST THOMAS' NHS FOUNDATION TRUST   (United Kingdom)

^h UNIVERSITY OF PITTSBURGH   (United States)

ⁱ ST GEORGE S HOSPITAL   (United Kingdom)

^j VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^k UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^l HARVARD MEDICAL SCHOOL   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BREAST TUMOR; CHROMOSOME 10; CHROMOSOME DELETION; CHROMOSOME MAP; COMPUTER PROGRAM; CONGENITAL TUMOR; FEMALE; GENETIC LINKAGE; GENETIC MARKER; GENETIC POLYMORPHISM; GENETICS; HUMAN; MALE; PEDIGREE; RISK FACTOR;

BREAST NEOPLASMS; CHROMOSOME DELETION; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; FEMALE; GENETIC MARKERS; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; PEDIGREE; POLYMORPHISM, GENETIC; RISK FACTORS; SOFTWARE;

EID: 0030140025     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0596-114     Document Type: Article

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