Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutations

Endocrine

Volumn 23, Issue 1, 2004, Pages 45-49

  Sakurai, Akihiro ^a,b   Katai, Miyuki ^a   Yumita, Wataru ^a   Minemura, Kesami ^a   Hashizume, Kiyoshi ^a  

^a SHINSHU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Incidentaloma; Multiple endocrine neoplasia type 1; Phenocopy

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUMAN CELL; HYPERPARATHYROIDISM; MULTIPLE ENDOCRINE NEOPLASIA; PHENOTYPE; PRIORITY JOURNAL;

EID: 2442465962     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1385/ENDO:23:1:45     Document Type: Article

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