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Journal Abstract Search

152 related items for PubMed ID: 4192207

  • 1. Infantile metachromatic leukodystrophy.
    Kaback MM, Howell RR.
    N Engl J Med; 1970 Jun 11; 282(24):1336-40. PubMed ID: 4192207
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  • 3. Infantile metachromatic leukodystrophy. Confirmation of a prenatal diagnosis.
    Leroy JG, Van Elsen AF, Martin JJ, Dumon JE, Hulet AE, Okada S, Navarro C.
    N Engl J Med; 1973 Jun 28; 288(26):1365-9. PubMed ID: 4707419
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  • 6. Prenatal genetic diagnosis (second of three parts).
    Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L.
    N Engl J Med; 1970 Dec 24; 283(26):1441-7. PubMed ID: 4098222
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  • 11. Role of amniocentesis in the intrauterine detection of genetic disorders.
    Nadler HL, Gerbie AB.
    N Engl J Med; 1970 Mar 12; 282(11):596-9. PubMed ID: 4244215
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  • 12. Leukodystrophy: diffuse cerebral sclerosis or Schilder's disease revisited.
    Norman MG.
    Perspect Pediatr Pathol; 1975 Mar 12; 2():61-100. PubMed ID: 48227
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  • 17. Prenatal genetic diagnosis. I.
    Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L.
    N Engl J Med; 1970 Dec 17; 283(25):1370-81. PubMed ID: 4921307
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  • 18. Deficiency of arylsulfatase A in juvenile metachromatic leucodystrophy: fibroblast studies.
    Leroy JG, Van Elsen A, Dumon JE, Radermecker J.
    Monogr Hum Genet; 1972 Dec 17; 6():148-9. PubMed ID: 4663890
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  • 19. Late adult metachromatic leukodystrophy. Arylsulfatase A activity of leukocytes in two families.
    Pilz H.
    Arch Neurol; 1972 Jul 17; 27(1):87-90. PubMed ID: 5049684
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  • 20. Enzymatic abnormality of the carrier state in metachromatic leukodystrophy.
    Taniguchi N, Nanba I.
    Clin Chim Acta; 1970 Sep 17; 29(3):375-9. PubMed ID: 5496557
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