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Journal Abstract Search

299 related items for PubMed ID: 5314298

  • 21. The human Y chrosome and the etiology of true hermaphroditism with the report of a case with XX-XY sex chromosome mosaicism.
    Brogger A, Aagenaes O.
    Hereditas; 1965; 53(1):231-46. PubMed ID: 5889237
    [No Abstract] [Full Text] [Related]

  • 22. [Study of a 46,XX-46,XX,17r mosaicism].
    Petit P, Koulischer L.
    Ann Genet; 1971 Mar; 14(1):55-8. PubMed ID: 5314296
    [No Abstract] [Full Text] [Related]

  • 23. Familial structural chromosome abnormality with maternal mosaicism.
    Insley J, McDermott A, Parrington J.
    Ann Genet; 1968 Sep; 11(3):138-44. PubMed ID: 5304613
    [No Abstract] [Full Text] [Related]

  • 24. Mosaicism of C-chromosome (6-12), 46, XY-45, XY, C. Report of four cases.
    Sillanpää M, Salonius AL.
    Acta Paediatr Scand Suppl; 1970 Sep; 206():Suppl 206:138+. PubMed ID: 5276956
    [No Abstract] [Full Text] [Related]

  • 25. [Chromosome anomalies].
    Tsuboi T, Asaka A.
    Shinkei Kenkyu No Shimpo; 1968 Sep; 12(1):83-96. PubMed ID: 4235569
    [No Abstract] [Full Text] [Related]

  • 26. [Translocation 46,XY,t(2;5) (q37;q14) and mental retardation. Clinical and cytogenetic study].
    Gilgenkrantz S, Walbaum R, Mauuary G, Pierson M.
    J Genet Hum; 1976 Mar; 24(1):27-37. PubMed ID: 58967
    [Abstract] [Full Text] [Related]

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  • 29. [Partial trisomy for the long arm of a C chromosome (?6) through t(Gp+;Cqs+) translocation].
    de Grouchy J, Emerit I, Aicardi J.
    Ann Genet; 1969 Jun; 12(2):133-7. PubMed ID: 5308386
    [No Abstract] [Full Text] [Related]

  • 30. A de novo tandem duplication 15(q21 leads to qter) mosaic.
    Yip MY, Parsons A, Hultén M.
    Clin Genet; 1982 Jul; 22(1):1-6. PubMed ID: 7172470
    [No Abstract] [Full Text] [Related]

  • 31. [A chemical and karyological study in a case of dyscraniotic oligophrenia].
    Caldarini G, Paracchi G.
    Folia Hered Pathol (Milano); 1968 Jul; 17(3):103-12. PubMed ID: 5732581
    [No Abstract] [Full Text] [Related]

  • 32. 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]

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  • 35. Mosaic supernumerary small ring chromosome.
    Fryns JP, van Herck G, van den Berghe H.
    J Genet Hum; 1981 Jun; 29(2):151-4. PubMed ID: 7328409
    [No Abstract] [Full Text] [Related]

  • 36. [Lethal chromosome abnormalities in the antenatal and perinatal stages of human development].
    Petrov-Maslakov MA, Golovachev GD.
    Vestn Akad Med Nauk SSSR; 1972 Jun; 27(5):68-77. PubMed ID: 5074593
    [No Abstract] [Full Text] [Related]

  • 37. [Mosaic structural anomaly of chromosome G in a boy with developmental defects].
    Dziekanowska D, Dziuba P, Bulsiewicz-Ciemniewska H, Rzeszotarska A.
    Pol Tyg Lek; 1970 Dec 07; 25(49):1901-3. PubMed ID: 5492689
    [No Abstract] [Full Text] [Related]

  • 38. A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.
    Short EM, Solitare GB, Breg WR.
    J Med Genet; 1972 Sep 07; 9(3):367-73. PubMed ID: 5079109
    [No Abstract] [Full Text] [Related]

  • 39. [On three cases of C trisomy].
    Lejeune J, Dutrillaux B, Rethoré MO, Berger R, Debray H, Veron P, Gorce F, Grossiord A.
    Ann Genet; 1969 Mar 07; 12(1):28-35. PubMed ID: 5306709
    [No Abstract] [Full Text] [Related]

  • 40. XY/XXY mosaicism and fragile X syndrome.
    Fryns JP, Kleczkowska A, Kubień E, Petit P, Haspeslagh M, Lindemans I, Van Den Berghe H.
    Ann Genet; 1983 Mar 07; 26(4):251-3. PubMed ID: 6607708
    [Abstract] [Full Text] [Related]

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