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PUBMED FOR HANDHELDS

Journal Abstract Search


125 related items for PubMed ID: 3914443

  • 1. [DNA diagnosis of genetic disease].
    Sakaki Y.
    Fukuoka Igaku Zasshi; 1985 Nov; 76(11):524-6. PubMed ID: 3914443
    [No Abstract] [Full Text] [Related]

  • 2. [Use of DNA polymorphism in the diagnosis of human genetic diseases].
    Cebrat S.
    Postepy Hig Med Dosw; 1988 Nov; 42(5):461-82. PubMed ID: 2908211
    [No Abstract] [Full Text] [Related]

  • 3. [Familial amyloidosis].
    Murakami T, Maeda S.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):950-4. PubMed ID: 3270914
    [No Abstract] [Full Text] [Related]

  • 4. The application of recombinant DNA methodology to the diagnosis of inherited disease.
    Cooper DN.
    Contrib Gynecol Obstet; 1986 Apr; 15():90-103. PubMed ID: 3017631
    [No Abstract] [Full Text] [Related]

  • 5. Recombinant DNA technology in prenatal diagnosis.
    Gosden JR, Gosden CM.
    Oxf Rev Reprod Biol; 1985 Apr; 7():73-117. PubMed ID: 3001618
    [No Abstract] [Full Text] [Related]

  • 6. [Prenatal diagnosis by DNA analysis].
    Kaplan JC, Delpech M.
    Rev Prat; 1987 Oct 29; 37(43):2595-611. PubMed ID: 3423671
    [No Abstract] [Full Text] [Related]

  • 7. Looking at genes.
    Kronenberg HM.
    N Engl J Med; 1982 Jul 01; 307(1):50-2. PubMed ID: 6281646
    [No Abstract] [Full Text] [Related]

  • 8. [Prenatal diagnosis of genetic disorders by linkage analysis (author's transl)].
    Sperling K.
    Wien Klin Wochenschr; 1982 Apr 16; 94(8):199-204. PubMed ID: 6954763
    [Abstract] [Full Text] [Related]

  • 9. [Diagnosis of genetic diseases using DNA recombination technics].
    Jungerman M, Witt M, Słomski R.
    Pol Tyg Lek; 1988 Sep 26; 43(39):1243-6. PubMed ID: 2907621
    [No Abstract] [Full Text] [Related]

  • 10. [DNA diagnosis of familial amyloidotic polyneuropathy].
    Sakaki Y, Sasaki H.
    Rinsho Byori; 1985 Nov 26; 33 Spec No 65():134-9. PubMed ID: 3912561
    [No Abstract] [Full Text] [Related]

  • 11. [Perinatal period. b. Prenatal diagnosis by genetic analysis].
    Suzumori K.
    Nihon Sanka Fujinka Gakkai Zasshi; 1994 Aug 26; 46(8):809-19. PubMed ID: 8089617
    [No Abstract] [Full Text] [Related]

  • 12. A recombinant DNA diagnostic program in practice.
    Hejtmancik JF, Harris SG, Ward PA, Caskey CT.
    Ann Clin Res; 1986 Aug 26; 18(5-6):250-5. PubMed ID: 2882727
    [No Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of hereditary amyloidosis in a Portuguese family.
    Morris M, Nichols W, Benson M.
    Am J Med Genet; 1991 Apr 01; 39(1):123-4. PubMed ID: 1867256
    [Abstract] [Full Text] [Related]

  • 14. Genetic basis for familial amyloidotic polyneuropathy.
    Shimada K, Maeda S, Araki S.
    Bioessays; 1986 May 01; 4(5):208-12. PubMed ID: 3790120
    [No Abstract] [Full Text] [Related]

  • 15. Molecular genetics for the clinician.
    Lancet; 1984 Feb 04; 1(8371):257-9. PubMed ID: 6142998
    [No Abstract] [Full Text] [Related]

  • 16. [Finnish hereditary amyloidosis: a mutation in the gelsolin gene].
    Maury P.
    Duodecim; 1994 Feb 04; 110(7):675-80. PubMed ID: 8542822
    [No Abstract] [Full Text] [Related]

  • 17. Amplification methods in the molecular diagnosis of genetic diseases.
    Ben-Ezra JM.
    Clin Lab Med; 1995 Dec 04; 15(4):795-815. PubMed ID: 8838224
    [Abstract] [Full Text] [Related]

  • 18. [DNA diagnosis of amyloidoses].
    Nishiguchi S, Murakami T, Araki S.
    Rinsho Byori; 1990 Jun 04; Suppl 85():72-81. PubMed ID: 2214213
    [No Abstract] [Full Text] [Related]

  • 19. [The use of DNA recombination technics in human genetics].
    Słomski R, Zietkiewicz E.
    Postepy Biochem; 1987 Jun 04; 33(4):451-71. PubMed ID: 2898138
    [No Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis for late-onset disease--always room for discussion.
    Cox SM, Yew S, Nisker J.
    Fertil Steril; 2005 Jun 04; 83(6):1887-8; author reply 1888. PubMed ID: 15950678
    [No Abstract] [Full Text] [Related]


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