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PUBMED FOR HANDHELDS

Journal Abstract Search


145 related items for PubMed ID: 589852

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  • 48. Partial trisomy 12q associated with a familial translocation.
    Hemming L, Brown R.
    Clin Genet; 1979 Jul; 16(1):25-8. PubMed ID: 477011
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  • 52. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
    Zhu CJ, Huang ZY, Wu WQ, Zhao Q, Jiang HY, Xie JS.
    Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
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  • 53. Probable pericentric inversion in chromosome no. 1 in a female child (46,XX,inv(Ip+q-).
    Mikelsaar AV, Ananjev EV, Gindilis VM.
    Humangenetik; 1970 Jun; 9(4):316-24. PubMed ID: 5449945
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  • 54. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
    Jacobsen P, Hauge M, Henningsen K, Hobolth N, Mikkelsen M, Philip J.
    Hum Hered; 1973 Jun; 23(6):568-85. PubMed ID: 4134631
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  • 55. An unusual chromosomal segregation in a family with a translocation between chromosomes 3 and 12.
    Sachdeva S, Smith GF, Justice P.
    J Med Genet; 1974 Sep; 11(3):303-5. PubMed ID: 4139264
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  • 59. [Case of partial trisomy 4p+ in a child as a result of a balanced translocation in the father].
    Patiutko RS, Kulieva LM, Egolina NA.
    Genetika; 1978 Sep; 14(9):1653-7. PubMed ID: 720831
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  • 60. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.
    Rosenthal IM, Krmpotic E, Bocian M, Szego K.
    Clin Genet; 1973 Jun; 4(6):507-16. PubMed ID: 4787842
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