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Volumn , Issue SUPPL. 62, 2009, Pages

Internet resources in medical genetics

Author keywords

Genetic counseling; Genetic testing; Medical genetics

Indexed keywords

ACCESS TO INFORMATION; CONSUMER ADVOCACY; DIFFERENTIAL DIAGNOSIS; GENE MAPPING; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC COUNSELING; GENOTYPE PHENOTYPE CORRELATION; HEREDITY; INFORMATION SYSTEM; INTERNET; MEDICAL GENETICS; MEDICAL SOCIETY; MICROARRAY ANALYSIS; MOLECULAR GENETICS; MOLECULAR MECHANICS; NEWBORN SCREENING; PATIENT CARE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW;

EID: 67651095588     PISSN: 19348266     EISSN: 19348258     Source Type: Journal    
DOI: 10.1002/0471142905.hg0912s62     Document Type: Review
Times cited : (6)

References (4)
  • 1
    • 0034022925 scopus 로고    scopus 로고
    • OMIM passes the 1,000 disease-gene mark
    • Antonarakis, S.E. and McKusick, V.A. 2000. OMIM passes the 1,000 disease-gene mark. Nat. Genet. 25:11.
    • (2000) Nat. Genet. , vol.25 , pp. 11
    • Antonarakis, S.E.1    McKusick, V.A.2
  • 2
    • 13444266370 scopus 로고    scopus 로고
    • Online Mendelian inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
    • Hamosh, A., Scott, A.F., Amberger, J.S., Bocchini, C.A., and McKusick, V.A. 2005. Online Mendelian inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res. 33:D514-D517.
    • (2005) Nucleic Acids Res. , vol.33
    • Hamosh, A.1    Scott, A.F.2    Amberger, J.S.3    Bocchini, C.A.4    McKusick, V.A.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.