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Volumn 24, Issue 3, 1986, Pages 513-518

Maternal Hartnup disorder

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID TRANSPORT; ATAXIA; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CENTRAL NERVOUS SYSTEM; CHILD; CONGENITAL DISORDER; DIAGNOSIS; ETIOLOGY; HARTNUP DISEASE; HEREDITY; HUMAN; HYDROCEPHALUS; INBORN ERROR OF METABOLISM; INTELLIGENCE QUOTIENT; MATERNAL DISEASE; MENTAL DEFICIENCY; NEURAL TUBE DEFECT; PRIORITY JOURNAL; PROGENY;

EID: 0022498090     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320240314     Document Type: Article
Times cited : (7)

References (18)
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  • 2
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  • 3
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    • Hartnup disease, in: The Metabolic Basis of Inherited Disease
    • Jepson JB (1978): Hartnup disease. In Stanbury, JB, Wyngaarden, JB, Frederickson, DS, (eds): “ The Metabolic Basis of Inherited Disease.” Fourth Ed. New York: McGraw Hill, pp 1563–1577.
    • (1978) , pp. 1563-1577
    • Jepson, JB1
  • 4
    • 85121080572 scopus 로고
    • Selected metabolic diseases, in: Genetic Diseases in Pregnancy: Maternal Effects and Fetal Outcome
    • Lamon JM, Lenke RR, Levy HL, Schulman JD, Shih VE (1981): Selected metabolic diseases. In Schulman, JD, Simpson, JL, (eds): “ Genetic Diseases in Pregnancy: Maternal Effects and Fetal Outcome.” New York: Academic Press, pp 1–55.
    • (1981) , pp. 1-55
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  • 5
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  • 7
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    • Genetic screening
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  • 8
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  • 9
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  • 10
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  • 11
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  • 12
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    • Prospective study of suspected associations between certain drugs administered during early pregnancy and congenital malformations
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  • 13
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  • 15
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  • 17
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  • 18
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    • Young, M1    Prenton, MA2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.