Allelic imbalance, including deletion of PTEN/MMACI, at the cowden disease locus on 10q22-23, in hamartomas from patients with cowden syndrome and germline PTEN mutation

Genes Chromosomes and Cancer

Volumn 21, Issue 1, 1998, Pages 61-69

  Marsh, Debbie J ^a   Dahia, Patricia L M ^a   Coulon, Valérie ^b   Zheng, Zimu ^a   Dorion Bonnet, Françoise ^b   Call, Katherine M ^c   Little, Randall ^c   Lin, Albert Y ^d   Eeles, Rosalind A ^e   Goldstein, Alisa M ^d   Hodgson, Shirley V ^f   Richardson, Anne Louise ^g   Robinson, Bruce G ^g,h   Weber, H Christian ^d   Longy, Michel ^b   Eng, Charis ^a,i,j  

^a HARVARD MEDICAL SCHOOL   (United States)

^b INSTITUT BERGONIÉ   (France)

^c GENOME THERAPEUTICS CORPORATION   (United States)

^d NATIONAL CANCER INSTITUTE   (United States)

^e INSTITUTE OF CANCER RESEARCH   (United Kingdom)

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

^g ROYAL NORTH SHORE HOSPITAL   (Australia)

^h UNIVERSITY OF SYDNEY   (Australia)

ⁱ UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^j DANA FARBER CANCER INSTITUTE   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 10Q; CLINICAL ARTICLE; CONTROLLED STUDY; COWDEN SYNDROME; GENE DELETION; GENE LOCUS; HAMARTOMA; HETEROZYGOSITY LOSS; HUMAN; HUMAN TISSUE; MISSENSE MUTATION; NONSENSE MUTATION; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

CHROMOSOMES, HUMAN, PAIR 10; FEMALE; GENE DELETION; GERM-LINE MUTATION; HAMARTOMA SYNDROME, MULTIPLE; HAPLOTYPES; HUMANS; LOSS OF HETEROZYGOSITY; MALE; PEDIGREE; PHOSPHORIC MONOESTER HYDROLASES; PROTEIN-TYROSINE-PHOSPHATASE; PTEN PHOSPHOHYDROLASE; TUMOR SUPPRESSOR PROTEINS;

EID: 0031974752     PISSN: 10452257     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-2264(199801)21:1<61::AID-GCC8>3.0.CO;2-6     Document Type: Article

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