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PUBMED FOR HANDHELDS

Journal Abstract Search


439 related items for PubMed ID: 6711595

  • 1. Fragile-X syndrome III: dermatoglyphic studies in males.
    Simpson NE, Newman BJ, Partington MW.
    Am J Med Genet; 1984 Jan; 17(1):195-207. PubMed ID: 6711595
    [Abstract] [Full Text] [Related]

  • 2. Dermatoglyphic findings in patients with fragile X-chromosome.
    Hirth L, Singh S, Schilling S, Müller E, Goedde HW.
    Clin Genet; 1985 Feb; 27(2):118-21. PubMed ID: 3978845
    [Abstract] [Full Text] [Related]

  • 3. The fragile X syndrome I: familial variation in the proportion of lymphocytes with the fragile site in males.
    Soudek D, Partington MW, Lawson JS.
    Am J Med Genet; 1984 Jan; 17(1):241-52. PubMed ID: 6711598
    [Abstract] [Full Text] [Related]

  • 4. Dermatoglyphics in 46, XY females.
    Bosco JI, Rajangam S, Shankar J, Thomas IM.
    J Indian Med Assoc; 2001 Aug; 99(8):418-20. PubMed ID: 11881854
    [Abstract] [Full Text] [Related]

  • 5. Dermatoglyphic indices of males with the fragile X syndrome and of the female heterozygotes.
    Simpson NE.
    Am J Med Genet; 1986 Aug; 23(1-2):171-8. PubMed ID: 3953645
    [Abstract] [Full Text] [Related]

  • 6. [X chromosome-linked mental retardation with fragile X chromosome and macro-orchidism].
    Zollinger A, Schmid W, Vilan J, Sorg B, Knoblauch M.
    Schweiz Med Wochenschr; 1983 Feb 19; 113(7):238-44. PubMed ID: 6836249
    [Abstract] [Full Text] [Related]

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  • 8. [Clinical and molecular screening for fragile X syndrome in 300 patients with non-specific mental retardation].
    Jara L, López M, Mellado C, Aspillaga M, Avendaño I, Blanco R.
    Rev Med Chil; 1998 Aug 19; 126(8):911-8. PubMed ID: 9830742
    [Abstract] [Full Text] [Related]

  • 9. [Screening for fragile X syndrome in handicapped boys].
    Steinbicker V, Missbach D, Goetz P, Subrt I, Seemanová E.
    Kinderarztl Prax; 1992 Aug 19; 60(6):163-7. PubMed ID: 1405391
    [Abstract] [Full Text] [Related]

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  • 11. Autistic features, personality, and adaptive behavior in males with the fragile X syndrome and no autism.
    Kerby DS, Dawson BL.
    Am J Ment Retard; 1994 Jan 19; 98(4):455-62. PubMed ID: 8148122
    [Abstract] [Full Text] [Related]

  • 12. Familial X-linked mental retardation syndrome associated with minor congenital anomalies, macro-orchidism, and fragile X-chromosome.
    Pueschel SM, Hays RM, Mendoza T.
    Am J Ment Defic; 1983 Jan 19; 87(4):372-6. PubMed ID: 6829615
    [Abstract] [Full Text] [Related]

  • 13. Discriminant analysis of dermatoglyphic measurements in fragile X males and females.
    Loesch DZ.
    Clin Genet; 1988 Mar 19; 33(3):169-75. PubMed ID: 3359677
    [Abstract] [Full Text] [Related]

  • 14. A dermatoglyphic study of a group of Sicilian children with fragile-X syndrome.
    Milone G, Conti L, Rizzo R, Sanfilippo S, Sammito V, Romano C.
    Am J Med Genet; 1988 Mar 19; 30(1-2):177-83. PubMed ID: 3177443
    [Abstract] [Full Text] [Related]

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  • 16. Fragile X-linked mental retardation, a new entity: case reports.
    Kelly TE, Shires MA, Harris L, Wyandt H, Wilson WG.
    Va Med; 1983 Apr 19; 110(4):250-2. PubMed ID: 6868782
    [No Abstract] [Full Text] [Related]

  • 17. [Mental retardation linked to fragility of chromosome X: current knowledge].
    Mattei JF, Mattei MG, Auger M, Giraud F.
    J Genet Hum; 1984 Jul 19; 32(3):167-92. PubMed ID: 6237176
    [Abstract] [Full Text] [Related]

  • 18. [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 19; 21 Suppl 20():54-7. PubMed ID: 6595955
    [No Abstract] [Full Text] [Related]

  • 19. Implications of fragile X expression in normal males for the nature of the mutation.
    Ledbetter DH, Ledbetter SA, Nussbaum RL.
    Nature; 1984 Oct 19; 324(6093):161-3. PubMed ID: 3785381
    [Abstract] [Full Text] [Related]

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