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Journal Abstract Search

107 related items for PubMed ID: 4248910

  • 1. [Incomplete G G translocation in a mongoloid girl].
    Schwanitz G, Meyer-Robisch M.
    Folia Clin Int (Barc); 1969 Sep; 19(9):448-50. PubMed ID: 4248910
    [No Abstract] [Full Text] [Related]

  • 2. [Cytogenetic and dermatoglyphic studies in Down's syndrome with G-G translocation].
    Trebicka-Kwiatkowska B, Raczkiewicz B, Galińska I, Gasiorowski A.
    Pol Tyg Lek; 1973 Aug 06; 28(32):1220-2. PubMed ID: 4270748
    [No Abstract] [Full Text] [Related]

  • 3. [Down's syndrome with G/G "tandem" translocation (author's transl)].
    López Pajares I, Barreiro E, Delicado A.
    An Esp Pediatr; 1976 Aug 06; 9(5):553-7. PubMed ID: 136915
    [Abstract] [Full Text] [Related]

  • 4. [Familial mongolism with G-G translocation in the karyotype].
    Hübner H, Jeske J, Dzida J.
    Pol Tyg Lek; 1969 Oct 06; 24(40):1539-41. PubMed ID: 4243796
    [No Abstract] [Full Text] [Related]

  • 5. Unusual chromosome aberrations in 3 children with Down syndrome.
    Osztovics M, Tóth S, Wilhelm O.
    Acta Paediatr Acad Sci Hung; 1982 Oct 06; 23(3):283-9. PubMed ID: 6217717
    [Abstract] [Full Text] [Related]

  • 6. Familial Down's syndrome with G-G translocation.
    Hubner H, Jeske J, Dzida J.
    Pol Med Sci Hist Bull; 1969 Oct 06; 12(4):164-7. PubMed ID: 4257690
    [No Abstract] [Full Text] [Related]

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  • 10. Probable reciprocal translocation in somatic cells from patients with Down's syndrome.
    Sonta S, Oishi H.
    Jinrui Idengaku Zasshi; 1974 Sep 06; 19(2):169-73. PubMed ID: 4280457
    [No Abstract] [Full Text] [Related]

  • 11. [Functional analysis of chromosome translocation (DqGq) in hereditary Down's syndrome by DNA replication pattern].
    Abe T.
    Saishin Igaku; 1968 Feb 10; 24(2):313-6. PubMed ID: 4239275
    [No Abstract] [Full Text] [Related]

  • 12. Familial translocation (3?--;G?- q+) and nondisjunction of chromosome in group G in two unrelated families.
    Soukup SW, Passarge E, Becroft DM, Shaw RL, Young LG.
    Cytogenetics; 1969 Feb 10; 8(5):315-25. PubMed ID: 4242066
    [No Abstract] [Full Text] [Related]

  • 13. Familial translocation (3?--;G?q+) and nondisjunction of chromosome in group G in two unrelated families.
    Soikup SW, Passarge E, Becroft SM, Shaw RL, Young LG.
    Cytogenetics; 1969 Feb 10; 8(4):315-25. PubMed ID: 4245463
    [No Abstract] [Full Text] [Related]

  • 14. [A study of the offspring of t(21q Dq) translocation carriers].
    Dutrillaux B, Lejeune J.
    Ann Genet; 1969 Jun 10; 12(2):77-82. PubMed ID: 4243780
    [No Abstract] [Full Text] [Related]

  • 15. A peculiar t(21 ; 14) translocation, associated with a pericentric inversion of the Y chromosome in a mongol boy.
    Orye E, Verhaaren H.
    Ann Genet; 1974 Sep 10; 17(3):217-20. PubMed ID: 4141590
    [No Abstract] [Full Text] [Related]

  • 16. [Incidence of association of acrocentric chromosomes].
    Krajewska-Walasek M.
    Pediatr Pol; 1980 Jan 10; 55(1):9-14. PubMed ID: 6445056
    [No Abstract] [Full Text] [Related]

  • 17. [Report on a case of Down's syndrome with mosaicism. Trisomy 21-normal, clearly mongoloid phenotype and normal iliac index in a newborn infant].
    De Prà M, Lunetta Q.
    Minerva Pediatr; 1974 Jan 28; 26(2):78-81. PubMed ID: 4276194
    [No Abstract] [Full Text] [Related]

  • 18. [Infant with free trisomy 21 and maternal t(14q 22q) translocation].
    Forabosco A, Dutrillaux B, Toni G, Lejeune J.
    Ann Genet; 1973 Mar 28; 16(1):57-9. PubMed ID: 4269148
    [No Abstract] [Full Text] [Related]

  • 19. [Congenital leukemia with chromosome aberrations (Trisomy G) in a non-mongoloid child].
    Bjönness H, Bühler EM, Fricker H, Gugler E.
    Helv Paediatr Acta; 1974 Nov 28; 29(5):457-70. PubMed ID: 4281418
    [No Abstract] [Full Text] [Related]

  • 20. [Mosaic of G-G translocation observed in a girl with faint symptoms of mongolism].
    Grosse KP, Schwanitz G, Grosse G, Mayer HP.
    Humangenetik; 1971 Nov 28; 13(4):315-9. PubMed ID: 4257569
    [No Abstract] [Full Text] [Related]

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