Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN

Journal of Medical Genetics

Volumn 36, Issue 5, 1999, Pages 360-364

  Çelebi, Julide Tok ^a   Tsou, Hui C ^a   Chen, Fei Fei ^a   Zhang, Hong ^a   Ping, Xiao Li ^a   Lebwohl, Mark G ^b   Kezis, Jeffrey ^a   Peacocke, Monica ^a  

^a Howard Hughes Medical Institute   (United States)

^b MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

Bannayan Zonana syndrome; Cowden syndrome; PTEN

Indexed keywords

ADULT; ALLELISM; ARTICLE; BANNAYAN ZONANA SYNDROME; CASE REPORT; CHILD; CLINICAL FEATURE; COWDEN SYNDROME; DISEASE PREDISPOSITION; FAMILY; FEMALE; GENE MUTATION; GERM LINE; HAMARTOMA; HUMAN; MALE; PHENOTYPE; PRIORITY JOURNAL; TUMOR SUPPRESSOR GENE;

ADULT; CHILD; CRANIOFACIAL ABNORMALITIES; FEMALE; GERM-LINE MUTATION; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; MALE; MIDDLE AGED; PEDIGREE; PHENOTYPE; PHOSPHORIC MONOESTER HYDROLASES; PTEN PHOSPHOHYDROLASE; SEQUENCE ANALYSIS, DNA; SYNDROME; TUMOR SUPPRESSOR PROTEINS;

EID: 0032922723     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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