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Journal Abstract Search

197 related items for PubMed ID: 6337391

  • 1. Recombinant DNA and the analysis of cytogenetic disorders associated with mental retardation.
    Gerald PS, Bruns GA.
    Res Publ Assoc Res Nerv Ment Dis; 1983; 60():173-9. PubMed ID: 6337391
    [No Abstract] [Full Text] [Related]

  • 2. Prader--Willi syndrome associated with an interstitial deletion of chromosome 15.
    Bonuccelli CM, Stetten G, Levitt RC, Levin LS, Pyeritz RE.
    Johns Hopkins Med J; 1982 Nov; 151(5):237-42. PubMed ID: 7143875
    [No Abstract] [Full Text] [Related]

  • 3. Fragile sites on chromosomes.
    Hecht F, Glover TW, Kaiser-Hecht B.
    Pediatrics; 1982 Jan; 69(1):121-3. PubMed ID: 6976555
    [No Abstract] [Full Text] [Related]

  • 4. 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; 87(4):372-6. PubMed ID: 6829615
    [Abstract] [Full Text] [Related]

  • 5. [Chromosomal pathology. Recent advances].
    Giraud F, Mattei JF.
    Arch Fr Pediatr; 1985 Mar; 42(3):159-62. PubMed ID: 2988476
    [No Abstract] [Full Text] [Related]

  • 6. [The clinico-genetic aspects of mental retardation related to the fragile-X chromosome].
    Viekhova NV, Demydova IA, Bychkova HM, Vorsanova SH, Buzhiievs'ka TI.
    Tsitol Genet; 1992 Mar; 26(6):64-71. PubMed ID: 1292164
    [Abstract] [Full Text] [Related]

  • 7. [Comparative analysis of the costs of cytogenetic techniques and molecular biology techniques in the diagnosis of fragile X disease].
    Hirtzlin I, Mandel JL, Lanoé JL, Fardeau-Gautier M.
    Rev Epidemiol Sante Publique; 1995 Mar; 43(3):205-14. PubMed ID: 7784670
    [Abstract] [Full Text] [Related]

  • 8. The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis.
    De Vries BB, Niermeijer MF.
    J Med Genet; 1994 Oct; 31(10):820. PubMed ID: 7837263
    [No Abstract] [Full Text] [Related]

  • 9. [The diagnosis of mental retardation in fragile X syndrome is revolutionized by molecular genetics].
    Lemire M, Rousseau F.
    Union Med Can; 1993 Oct; 122(1):23-9. PubMed ID: 8465472
    [Abstract] [Full Text] [Related]

  • 10. [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]

  • 11. New insights into the genetic basis of intellectual disabilities.
    Skellern C, Lennox N, Glass I.
    Aust Fam Physician; 2000 Jan 19; 29(1):41-5. PubMed ID: 10721542
    [Abstract] [Full Text] [Related]

  • 12. The fragile X chromosome: current methods.
    Hecht F, Jacky PB, Sutherland GR.
    Am J Med Genet; 1982 Apr 19; 11(4):489-95. PubMed ID: 6211983
    [No Abstract] [Full Text] [Related]

  • 13. Characterisation of a new rare fragile site easily confused with the fragile X.
    Sutherland GR, Baker E.
    Hum Mol Genet; 1992 May 19; 1(2):111-3. PubMed ID: 1301146
    [Abstract] [Full Text] [Related]

  • 14. The cytogenetic controversy regarding the Prader-Willi syndrome.
    Kousseff BG, Douglass R.
    Birth Defects Orig Artic Ser; 1982 May 19; 18(3B):301-4. PubMed ID: 6958334
    [No Abstract] [Full Text] [Related]

  • 15. [Chromosome characteristics of X-linked mental retardation. II. Autosomes].
    Bedel'baeva KhA, Baranovskaia LI, Zakharov AF.
    Genetika; 1987 Mar 19; 23(3):510-20. PubMed ID: 3569896
    [Abstract] [Full Text] [Related]

  • 16. Mental retardation, megalotestes and a marker X chromosome.
    Fitzsimmons J, McLachlan JI, Fitzsimmons E, Cooke P.
    Practitioner; 1982 Apr 19; 226(1366):735-41. PubMed ID: 6953399
    [No Abstract] [Full Text] [Related]

  • 17. X-linked mental retardation and fragile-X or marker-X syndrome.
    Rhoads FA.
    Pediatrics; 1982 May 19; 69(5):668-9. PubMed ID: 7079031
    [No Abstract] [Full Text] [Related]

  • 18. Molecular genetic approaches to human diseases involving mental retardation.
    Latt SA, Kurnit DM, Bruns GP, Schreck RR, Morton CC, Kunkel LM, Lalande M, Aldridge J, Neve R, Tantravahi U.
    Am J Ment Defic; 1984 Mar 19; 88(5):561-71. PubMed ID: 6731492
    [Abstract] [Full Text] [Related]

  • 19. On the nosology of moderate mental retardation with special attention to X-linked mental retardation. A diagnostic genetic survey of 274 institutionalized moderately mentally retarded men.
    Volcke P, Dereymaeker AM, Fryns JP, van den Berghe H.
    Genet Couns; 1990 Mar 19; 1(1):47-56. PubMed ID: 2222922
    [Abstract] [Full Text] [Related]

  • 20. [Mental retardation linked to the fragile X. Still questions...].
    Jalbert P.
    Pediatrie; 1983 Mar 19; 38(3):191-8. PubMed ID: 6379595
    [No Abstract] [Full Text] [Related]

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