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PUBMED FOR HANDHELDS

Journal Abstract Search


802 related items for PubMed ID: 4274010

  • 21.
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  • 23. [Indications for the examination of chromosomes in ophthalmology].
    Vrba M.
    Cesk Oftalmol; 1969 Sep; 25(5):304-6. PubMed ID: 4241557
    [No Abstract] [Full Text] [Related]

  • 24. Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders II. Cases 3,4 and 5.
    Moore MK, Engel E.
    Ann Genet; 1970 Jun; 13(2):129-34. PubMed ID: 5310697
    [No Abstract] [Full Text] [Related]

  • 25. Osseous malformations associated with chromosome abnormalities.
    Weiss L, Reynolds WA.
    Orthop Clin North Am; 1972 Nov; 3(3):713-32. PubMed ID: 4264453
    [No Abstract] [Full Text] [Related]

  • 26. Cytogenetics and the pathologist.
    Carr DH.
    Pathol Annu; 1975 Nov; 10():93-144. PubMed ID: 126409
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  • 27.
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  • 28. Autosomal chromosome aberrations in ophthalmology.
    Francois J.
    Int Ophthalmol Clin; 1968 Nov; 8(4):839-910. PubMed ID: 4244691
    [No Abstract] [Full Text] [Related]

  • 29. The antenatal diagnosis of genetic disease.
    Doran TA, Rudd NL, Gardner HA, Lowden JA, Benzie RJ, Liedgren SI.
    Am J Obstet Gynecol; 1974 Feb 01; 118(3):314-21. PubMed ID: 4272472
    [No Abstract] [Full Text] [Related]

  • 30. [The autosomal chromosome aberrations in ophthalmology].
    François J.
    J Genet Hum; 1966 Feb 01; 15():Suppl:133-208. PubMed ID: 4873685
    [No Abstract] [Full Text] [Related]

  • 31.
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  • 35. [Prenatal diagnosis of chromosome abnormalities. Three years of experience].
    Boue J, Boue A, Girard S, Thepot F.
    Arch Fr Pediatr; 1976 Feb 01; 33(7):653-64. PubMed ID: 999438
    [Abstract] [Full Text] [Related]

  • 36. Prenatal karyotype analysis in high risk families.
    Aula P, Karjalainen O.
    Ann Clin Res; 1973 Jun 01; 5(3):142-8. PubMed ID: 4127164
    [No Abstract] [Full Text] [Related]

  • 37. Cytogenetic survey of 504 mentally retarded individuals.
    Singh DN, Osborne RA, Paul JR, Catoe S, Katzberg A, Hennigar GR, Barnett CD.
    J Ment Defic Res; 1974 Dec 01; 18(4):293-305. PubMed ID: 4282744
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  • 38. [Identification of 2 familial translocations].
    Laurent C, Biemont MC, Robert JM, Dutrillaux B.
    Ann Genet; 1974 Dec 01; 17(4):279-81. PubMed ID: 4548825
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  • 39. [Prenatal diagnosis of hereditary diseases].
    Gunev V.
    Akush Ginekol (Sofiia); 1975 Dec 01; 14(4):322-9. PubMed ID: 130083
    [No Abstract] [Full Text] [Related]

  • 40. Prenatal diagnosis. Results of cytogenetic analysis of amniotic fluid cell cultures.
    Mulcahy MT, Jenkyn J.
    Med J Aust; 1973 May 19; 1(20):979-82. PubMed ID: 4268556
    [No Abstract] [Full Text] [Related]


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