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Volumn 3, Issue 4, 2001, Pages 290-293

Considerations for a multiaxis nomenclature system for medical genetics

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BECKWITH WIEDEMANN SYNDROME; CYSTIC FIBROSIS; DIAGNOSTIC PROCEDURE; DOWN SYNDROME; GENETIC ANALYSIS; GENETIC ASSOCIATION; HUMAN; MEDICAL GENETICS; MEDICAL PRACTICE; MEDICAL SOCIETY; NOMENCLATURE; ONSET AGE; PRACTICE GUIDELINE; PRADER WILLI SYNDROME; PROFESSIONAL STANDARD; RETINITIS PIGMENTOSA;

EID: 0035746504     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/00125817-200107000-00004     Document Type: Article
Times cited : (32)

References (16)
  • 2
    • 0031881532 scopus 로고    scopus 로고
    • Lumping and splitting: Molecular biology in the genetics clinic
    • (1998) Clin Genet , vol.53 , pp. 3-7
    • Biesecker, L.1
  • 10
    • 0034622122 scopus 로고    scopus 로고
    • A brief review of retinitis pigmentosa and the identified retinitis pigmentosa genes
    • (2000) Mol Vis , vol.6 , pp. 116-124
    • Phelan, J.K.1    Bok, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.