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Volumn 11, Issue 1, 2001, Pages 93-

Medullary thyroid carcinoma and lack of renal agenesis

Author keywords

[No Author keywords available]

Indexed keywords

GENE MUTATION; GENETIC ANALYSIS; HUMAN; KIDNEY AGENESIS; LETTER; MAJOR CLINICAL STUDY; MULTIPLE ENDOCRINE NEOPLASIA; PRIORITY JOURNAL; THYROID MEDULLARY CARCINOMA;

EID: 0035140379     PISSN: 10507256     EISSN: None     Source Type: Journal    
DOI: 10.1089/10507250150500739     Document Type: Letter
Times cited : (2)

References (5)
  • 3
    • 0023834887 scopus 로고
    • Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: A new autosomal recessive syndrome
    • (1988) J Med Genet , vol.25 , pp. 204-205
    • Santos, H.1    Mateus, J.2    Leal, M.J.3
  • 5
    • 0031941550 scopus 로고    scopus 로고
    • Molecular development of the kidney: A review of the results of gene disruption studies
    • (1998) Am J Kidney Dis , vol.31 , pp. 383-397
    • Lipschutz, J.H.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.