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Volumn 386, Issue 8, 2002, Pages 547-552

Clinical and molecular diagnosis of multiple endocrine neoplasia type 1

Author keywords

Genetics; MEN 1; Screening; Tumor suppressor

Indexed keywords

CLINICAL FEATURE; DIAGNOSTIC APPROACH ROUTE; DNA DETERMINATION; GENE ACTIVATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC SCREENING; HETEROZYGOTE; HUMAN; LEGAL ASPECT; MEDICAL ETHICS; MULTIPLE ENDOCRINE NEOPLASIA; PRIORITY JOURNAL; REVIEW; TUMOR SUPPRESSOR GENE;

EID: 0036211606     PISSN: 14352443     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00423-001-0268-4     Document Type: Review
Times cited : (15)

References (21)
  • 6
    • 0033947253 scopus 로고    scopus 로고
    • Multiple endocrine neoplasia type 1 (MEN1) gene mutations in a subset of patients with sporadic and familial primary hyperparathyroidism target the coding sequence but spare the promoter region
    • (2000) J Endocrinol , vol.166 , pp. 1-9
    • Karges, W.1    Jostarndt, K.2    Maier, S.3
  • 15
    • 8544279953 scopus 로고    scopus 로고
    • Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states
    • (1997) Hum Mol Genet , vol.6 , pp. 1169-1175
    • Agarwal, S.K.1
  • 17
  • 18
    • 0031871547 scopus 로고    scopus 로고
    • Genetic testing in multiple endocrine neoplasia and related syndromes
    • (1998) Forum Genova , vol.8 , pp. 146-159
    • Calender, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.