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Volumn 18, Issue 3, 2001, Pages 210-212

Rothmund-Thomson syndrome with myelodysplasia

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BONE DEFECT; CASE REPORT; CHILD; DISEASE ASSOCIATION; DNA REPAIR; ERYTHEMA; FACE MALFORMATION; HUMAN; KERATODERMA; MALE; MYELODYSPLASIA; NEUTROPENIA; OTITIS MEDIA; POIKILODERMA; PRIORITY JOURNAL; ROTHMUND THOMSON SYNDROME; SOFT TISSUE DISEASE;

EID: 0034972312     PISSN: 07368046     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1525-1470.2001.018003210.x     Document Type: Article
Times cited : (26)

References (18)
  • 10
    • 0029805236 scopus 로고    scopus 로고
    • Rothmund-Thomson syndrome: Two case reports show heterogeneous cutaneous abnormalities, an association with genetically programmed ageing changes, and increased chromosomal radiosensitivity
    • (1996) J Med Genet , vol.33 , pp. 928-934
    • Kerr, B.1    Ashcroft, G.S.2    Scott, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.