Carney complex, Peutz-Jeghers syndrome, Cowden disease, and Bannayan- Zonana syndrome share cutaneous and endocrine manifestations, but not genetic loci

Journal of Clinical Endocrinology and Metabolism

Volumn 83, Issue 8, 1998, Pages 2972-2976

  Stratakis, Constantine A ^a   Kirschner, Lawrence S ^a   Taymans, Susan E ^a   Tomlinson, Ian P M ^e   Marsh, Debbie J ^d   Torpy, David J ^a   Giatzakis, Christoforos ^a   Eccles, Diana M ^h   Theaker, Jeffrey ^h   Houlston, Richard S ^f   Blouin, Jean Louis ⁱ   Antonarakis, Stylianos E ⁱ   Basson, Craig T ^b   Eng, Charis ^d,g   Carney, J Aidan ^c  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b NEW YORK PRESBYTERIAN HOSPITAL   (United States)

^c MAYO CLINIC   (United States)

^d DANA FARBER CANCER INSTITUTE   (United States)

^e UNIVERSITY OF OXFORD   (United Kingdom)

^f INSTITUTE OF CANCER RESEARCH   (United Kingdom)

^g UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^h PRINCESS ANNE HOSPITAL   (United Kingdom)

ⁱ UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

ARTICLE; BANNAYAN ZONANA SYNDROME; CARNEY COMPLEX; CHROMOSOME 10Q; CHROMOSOME 19P; CHROMOSOME 19Q; CHROMOSOME 2P; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; COWDEN SYNDROME; ENDOCRINE TUMOR; FAMILIAL DISEASE; FEMALE; GENE LOCUS; GENETIC HETEROGENEITY; GENETIC LINKAGE; HETEROZYGOSITY LOSS; HUMAN; HUMAN CELL; HUMAN TISSUE; LENTIGINOSIS; MALE; PEUTZ JEGHERS SYNDROME; PHENOTYPE; PRIORITY JOURNAL; TUMOR CELL LINE; TUMOR SUPPRESSOR GENE;

EID: 14444280886     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jcem.83.8.5042     Document Type: Article

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