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Volumn 42, Issue 4, 2004, Pages 221-226

Neurodegenerative disease in infants with multiple congenital malformations - Report of two cases

Author keywords

4pter; Chromosomal aberration; Congenital malformations; Neurodegenerative disease; Prenatal onset growth deficiency

Indexed keywords

ARTICLE; AUTOPSY; BASAL GANGLION; BRAIN ATROPHY; BRAIN CELL; BRAIN CORTEX; BRAIN NERVE CELL; BRAIN SPONGIOSIS; CASE REPORT; CAUDATE NUCLEUS; CELL DEATH; CENTRAL NERVOUS SYSTEM; CHROMOSOME ABERRATION; CLINICAL FEATURE; CLINODACTYLY; DISEASE SEVERITY; EMBRYO DEVELOPMENT; EPICANTHUS; FEMALE; GENETIC ANALYSIS; GROWTH RETARDATION; HUMAN; HUMAN TISSUE; INFANT; INFANT DISEASE; INFANT MORTALITY; IRIS COLOBOMA; MULTIPLE MALFORMATION SYNDROME; NERVE DEGENERATION; PERINATAL PERIOD; PROTEIN FUNCTION; WHITE MATTER;

EID: 12344328447     PISSN: 16414640     EISSN: 1509572X     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (8)
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    • Anvret, M.1    Nordenskjold, M.2    Stolpe, L.3    Brondum-Nielsen, K.4
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    • Ellison, D.1    Love, S.2    Chimelli, L.3    Harding, B.N.4    Love, J.5    Vinters, H.V.6
  • 4
    • 0003436550 scopus 로고
    • Johns Hopkins University, Baltimore Wolf-Hirschhorn syndrome #194190. Online: www.ncbi.nlm.nih.gov/Omim
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  • 5
    • 0003436550 scopus 로고
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    • McKusick, V.A.1
  • 6
    • 0003436550 scopus 로고
    • Johns Hopkins University, Baltimore Huntington Disease #143100. Online: www.ncbi.nlm.nih.gov/Omim
    • McKusick VA. Mendelian Inheritance in Man. Johns Hopkins University, Baltimore (1966-2004): Huntington Disease #143100. Online: www.ncbi.nlm.nih.gov/Omim
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    • McKusick, V.A.1
  • 7
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    • Molecular genetic classification of central nervous system malformation
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    • Sarnat, B.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.