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Journal Abstract Search

158 related items for PubMed ID: 1870597

  • 61. Experience of an academic reference laboratory using automation for analysis of cystic fibrosis mutations.
    DeMarchi JM, Beaudet AL, Caskey CT, Richards CS.
    Arch Pathol Lab Med; 1994 Jan; 118(1):26-32. PubMed ID: 8285831
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  • 63. Effects of neonatal screening for cystic fibrosis on reproduction, attitudes toward reproductive behaviour and genetic knowledge.
    Dankert-Roelse JE, Knol K, ten Kate LP.
    Acta Univ Carol Med (Praha); 1990 Jan; 36(1-4):99-101. PubMed ID: 2130734
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  • 64. [Prenatal diagnosis of cystic fibrosis].
    Estivill X.
    An Esp Pediatr; 1988 Jul; 29(1):1-5. PubMed ID: 3190006
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  • 65. Current concepts in genetics. Cystic fibrosis.
    Bowman BH, Mangos JA.
    N Engl J Med; 1976 Apr 22; 294(17):937-8. PubMed ID: 943696
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  • 66. [DNA diagnosis of monogene hereditary diseases exemplified by phenylketonuria and mucoviscidosis].
    Trefz FK, Lichter-Konecki U, Krawczak M, Schmidtke J, Dueck M, Nützenadel W, Konecki DS.
    Monatsschr Kinderheilkd; 1989 Apr 22; 137(4):201-7. PubMed ID: 2659975
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  • 70. [Early detection, heterozygote diagnosis and prenatal diagnosis in cystic fibrosis (mucoviscidosis)].
    Hein J.
    Kinderarztl Prax; 1982 Apr 22; 50(4):186-95. PubMed ID: 7109464
    [No Abstract] [Full Text] [Related]

  • 71. [Prenatal diagnosis of cystic fibrosis].
    ten Kate LP.
    Tijdschr Kindergeneeskd; 1987 Apr 22; 55(2):53-63. PubMed ID: 2884752
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  • 75. Prenatal prediction of cystic fibrosis in a mother homozygous for the delta F508 mutation.
    Dahl N, Kollberg H.
    Clin Genet; 1992 Oct 22; 42(4):214-5. PubMed ID: 1424248
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