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

Journal Abstract Search


153 related items for PubMed ID: 3953644

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Investigation of the twinning rate in families with the fragile X syndrome.
    Sherman SL, Turner G, Sheffield L, Laing S, Robinson H.
    Am J Med Genet; 1988; 30(1-2):625-31. PubMed ID: 3177474
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. Sex chromosome aneuploidy in fragile X carriers.
    Nielsen KB.
    Am J Med Genet; 1986; 23(1-2):537-44. PubMed ID: 3953664
    [Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29. [Mental retardation with X fragility: Armenfrax. Review and personal studies].
    Engel E.
    Rev Med Suisse Romande; 1983 Apr; 103(4):333-44. PubMed ID: 6348915
    [No Abstract] [Full Text] [Related]

  • 30. The fragile X syndrome: variability of expression in carrier females.
    Howard-Peebles PN, Brown WT.
    Am J Med Genet; 1988 Apr; 30(1-2):227-30. PubMed ID: 3177448
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Clinical features and reproductive patterns in fragile X female heterozygotes.
    Loesch DZ, Hay DA.
    J Med Genet; 1988 Jun; 25(6):407-14. PubMed ID: 3398009
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38. Fragile X transmission and the determination of carrier probabilities for genetic counseling.
    Mulley JC, Sutherland GR.
    Am J Med Genet; 1987 Apr; 26(4):987-90. PubMed ID: 3591842
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation.
    Voelckel MA, Philip N, Piquet C, Pellissier MC, Oberlé I, Birg F, Mattei MG, Mattei JF.
    Hum Genet; 1989 Mar; 81(4):353-7. PubMed ID: 2564838
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 8.