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Journal Abstract Search

190 related items for PubMed ID: 4684369

  • 1. Duplication-deficiency product of a pericentric inversion in man: a cause of D 1 trisomy syndrome.
    Taysi K, Bobrow M, Balci S, Madan K, Atasu M, Say B.
    J Pediatr; 1973 Feb; 82(2):263-8. PubMed ID: 4684369
    [No Abstract] [Full Text] [Related]

  • 2. Partial monosomy and partial trisomy 18 in two offspring of carrier of pericentric inversion of chromosome 18.
    Vianna-Morgante AM, Nozaki MJ, Ortega CC, Coates V, Yamamura Y.
    J Med Genet; 1976 Oct; 13(5):366-70. PubMed ID: 1003448
    [Abstract] [Full Text] [Related]

  • 3. Patau's syndrome with D 1 duplication-deficenncy derived from a maternal D group pericentric inversion.
    Parrington JM, Edwards JH.
    Ann Hum Genet; 1971 Jul; 35(1):35-45. PubMed ID: 5106368
    [No Abstract] [Full Text] [Related]

  • 4. [Pure trisomy 13q13-qter caused by aneusomic recombination of a maternal pericentric inversion].
    Lucas J, Le Mée F, Picard F, Le Marec B, Junien C.
    Ann Genet; 1983 Jul; 26(3):187-90. PubMed ID: 6606383
    [Abstract] [Full Text] [Related]

  • 5. A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.
    Andersen O, Lundsteen C, Niebuhr E.
    Cytogenet Cell Genet; 1981 Jul; 30(1):3-10. PubMed ID: 7261680
    [Abstract] [Full Text] [Related]

  • 6. Inherited pericentric inversion of a group D (13-15) chromosome.
    Surana RB, Conen PE.
    J Med Genet; 1972 Mar; 9(1):105-10. PubMed ID: 5025473
    [No Abstract] [Full Text] [Related]

  • 7. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
    Butler LJ, Eades SM, France NE.
    Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
    [No Abstract] [Full Text] [Related]

  • 8. [Pericentric inversion of chromosome 4 : inv (4) (p13, q35) and trisomy of the short branch of chromosome 4 due to recombination aneusomy].
    Dallapiccola B, Capra L, Preto G, Covic M, Dutrillaux B.
    Ann Genet; 1974 Jun; 17(2):115-8. PubMed ID: 4547938
    [No Abstract] [Full Text] [Related]

  • 9. Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).
    Stoll C, Levy JM, Gardea A.
    Humangenetik; 1975 Jun; 27(3):269-74. PubMed ID: 1150249
    [No Abstract] [Full Text] [Related]

  • 10. Clinical experience with trisomies 18 and 13.
    Hodes ME, Cole J, Palmer CG, Reed T.
    J Med Genet; 1978 Feb; 15(1):48-60. PubMed ID: 637922
    [Abstract] [Full Text] [Related]

  • 11. [Partial trisomy C through a familial translocation t(Cq+;Cq-)].
    Lejeune J, Rethoré MO, Berger R, Abonyi D, Dutrillaux B, See G.
    Ann Genet; 1968 Sep; 11(3):171-5. PubMed ID: 5304617
    [No Abstract] [Full Text] [Related]

  • 12. Gene deletion and duplication effects on phenotype and gamma globulin levels.
    Rudd NL, Lamarche PH.
    J Med Genet; 1971 Mar; 8(1):97-106. PubMed ID: 5098075
    [No Abstract] [Full Text] [Related]

  • 13. [Double trisomy and transmitted pericentric inversion (48,XXY, +21,inv(22)). Interchromosomal effect].
    Saura R, Longy M, Sautarael M, Renouil M, Sandler B.
    Ann Genet; 1983 Mar; 26(3):180-2. PubMed ID: 6606381
    [Abstract] [Full Text] [Related]

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