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

178 related items for PubMed ID: 4268902

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 49.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 50. Newer procedures in the preconceptional, prenatal and early postnatal diagnosis of birth defects.
    Nadler HL.
    Birth Defects Orig Artic Ser; 1970 May; 6(1):26-33. PubMed ID: 5522716
    [No Abstract] [Full Text] [Related]

  • 51. A mentally retarded male with karyotype 47,XY, plus mar equal ?i (18p).
    Nielsen J, Hreidarsson AB, Berggreen S, Ried E, Tsuboi T, Saldaña-Garcia P.
    Ann Genet; 1974 Jun; 17(2):129-33. PubMed ID: 4547941
    [No Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53. Schinzel-Giedion syndrome. A patient with hypothyroidism and diabetes insipidus.
    Santos H, Cordeiro I, Medeira A, Mendonça E, Antunes NL, Rosa FC.
    Genet Couns; 1994 Jun; 5(2):187-9. PubMed ID: 7917131
    [Abstract] [Full Text] [Related]

  • 54. The incidence of developmental and other genetic abnormalities.
    Polani PE.
    Guys Hosp Rep; 1973 Jun; 122(1-2):53-63. PubMed ID: 4804330
    [No Abstract] [Full Text] [Related]

  • 55.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 56. A family with a presumptive C-F translocation in five generations.
    Therkelsen AJ, Klinge T, Henningsen K, Mikkelsen M, Schmidt G.
    Ann Genet; 1971 Mar; 14(1):13-21. PubMed ID: 5314290
    [No Abstract] [Full Text] [Related]

  • 57. [Rubinstein-Taybi syndrome (a propos of 4 cases)].
    Levy-Leblond E, D'Oelsnitz M, Vaillant JM, Maroteaux P.
    Arch Fr Pediatr; 1969 May; 26(5):523-35. PubMed ID: 5363526
    [No Abstract] [Full Text] [Related]

  • 58. The human simian crease and its variants. A model for investigation of serious congenital malformation.
    Hook EB, Bonenfant R, Powers ML, Greenberg M, Shapiro LR.
    Birth Defects Orig Artic Ser; 1974 May; 10(7):7-16. PubMed ID: 4420918
    [No Abstract] [Full Text] [Related]

  • 59. An introduction to cytogenetics in medicine and dentistry.
    Lustenberger AA, Shapiro LR.
    J Oral Med; 1974 May; 29(3):64-8. PubMed ID: 4276810
    [No Abstract] [Full Text] [Related]

  • 60. Genetic screening for mental retardation in Michigan.
    Thoene J, Higgins J, Krieger I, Schmickel R, Weiss L.
    Am J Ment Defic; 1981 Jan; 85(4):335-40. PubMed ID: 7457497
    [Abstract] [Full Text] [Related]

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