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


179 related items for PubMed ID: 3591842

  • 1. 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]

  • 2. Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14.
    Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR.
    Am J Med Genet; 1987 Jun; 27(2):435-48. PubMed ID: 2886048
    [Abstract] [Full Text] [Related]

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

  • 4. [Sex-related neurologic diseases. Familial X-linked mental retardation with a fragile X marker. Study of 8 families].
    Rodríguez Costa T, Gabarrón Llamas J, Casas Fernández C, Glover López G, Puche Mira A, Jiménez Cocina A.
    An Esp Pediatr; 1984 Oct; 21 Suppl 20():54-7. PubMed ID: 6595955
    [No Abstract] [Full Text] [Related]

  • 5. X-linked mental retardation.
    Fryns JP.
    Prog Clin Biol Res; 1985 Oct; 177():309-19. PubMed ID: 2409559
    [No Abstract] [Full Text] [Related]

  • 6. [Fragile X syndrome: what do we know today?].
    Ramos FJ.
    An Esp Pediatr; 1989 Nov; 31(5):417-9. PubMed ID: 2575879
    [No Abstract] [Full Text] [Related]

  • 7. Fragile X syndrome associated with Tourette symptomatology in a male with moderate mental retardation and autism.
    Kerbeshian J, Burd L, Martsolf JT.
    J Dev Behav Pediatr; 1984 Aug; 5(4):201-3. PubMed ID: 6590572
    [No Abstract] [Full Text] [Related]

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

  • 9. The fragile X syndrome.
    Brown WT.
    Neurol Clin; 1989 Feb; 7(1):107-21. PubMed ID: 2646518
    [Abstract] [Full Text] [Related]

  • 10. [(Fra)X in male cousins with mental retardation].
    Rozynkowa D, Górski G, Jabłońska R.
    Pediatr Pol; 1986 Jul; 61(7):441-5. PubMed ID: 3822610
    [No Abstract] [Full Text] [Related]

  • 11. Cytogenetic survey for autistic fragile X carriers in a mental retardation center.
    Cantú ES, Stone JW, Wing AA, Langee HR, Williams CA.
    Am J Ment Retard; 1990 Jan; 94(4):442-7. PubMed ID: 2297426
    [Abstract] [Full Text] [Related]

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

  • 13. A counseling guide to the Martin-Bell syndrome.
    Weaver DD, Sherman SL.
    Am J Med Genet; 1987 Jan; 26(1):39-44. PubMed ID: 3812576
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Questions about fragile X syndrome and mental retardation. Clinical and therapeutic aspects].
    Suerinck-Neoussikhin E, Noël B, Quack B, Bonnaure C, Nougier B, Moulin B, Bénézech M.
    Ann Med Psychol (Paris); 1989 Dec; 147(10):1071-7; discussion 1077-8. PubMed ID: 2637638
    [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. [Mental retardation and fragile X chromosome. Clinical and cytogenetic study of 3 families].
    Gilgenkrantz S, Boué J, Grégoire MJ, Tejada I.
    J Genet Hum; 1984 Jul; 32(3):199-207. PubMed ID: 6481342
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 9.