These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

121 related items for PubMed ID: 1982278

  • 1. Prenatal diagnosis of inherited hemoglobinopathies.
    Cao A, Pirastu M, Rosatelli C.
    Haematologica; 1990; 75 Suppl 5():169-77. PubMed ID: 1982278
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. First-trimester prenatal molecular diagnosis of infantile hypophosphatasia in a Japanese family.
    Orimo H, Nakajima E, Hayashi Z, Kijima K, Watanabe A, Tenjin H, Araki T, Shimada T.
    Prenat Diagn; 1996 Jun; 16(6):559-63. PubMed ID: 8809899
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Prenatal diagnosis for beta-thalassemia by PCR from single chorionic villus.
    Cariolou MA, Kokkofitou A, Manoli P, Ioannou P.
    Biotechniques; 1993 Jul; 15(1):32-4. PubMed ID: 8363835
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of inherited hemoglobinopathies.
    Cao A, Rosatelli C, Pirastu M.
    J Genet Hum; 1986 Nov; 34(5):413-24. PubMed ID: 3540210
    [Abstract] [Full Text] [Related]

  • 14. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S, Moine P, Sarda P, Lefort G, Boulot P, Demaille J, Claustres M.
    Genet Couns; 1994 Nov; 5(2):183-5. PubMed ID: 7917130
    [Abstract] [Full Text] [Related]

  • 15. [Prenatal diagnosis: molecular basis and techniques used in the diagnosis of monogenic hereditary diseases].
    Villegas Martínez A.
    An Med Interna; 1989 May; 6(5):227-9. PubMed ID: 2577487
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.