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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 5096547

  • 1. A child with a ring G chromosome (46,XX, Gr).
    Nevin NC, MacLaverty B, Campbell WA.
    J Med Genet; 1971 Jun; 8(2):231-4. PubMed ID: 5096547
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  • 4. An inherited small extra chromosome: a mother with 46,XX,t(17;22)(pl;ql) and a son with 47,XY,+der(22)mat.
    Borgaonkar DS, McKusick VA, Farber PA.
    J Med Genet; 1973 Dec; 10(4):379-84. PubMed ID: 4129973
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  • 5. Dicentric chromosome due to an unusual fusion.
    Subrt I, Blehová B, Táborský O.
    Humangenetik; 1971 Dec; 12(2):136-41. PubMed ID: 5568732
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  • 7. Monosomy G: case report and review of the literature.
    Greenwood RD, Sommer A.
    J Med Genet; 1971 Dec; 8(4):496-500. PubMed ID: 5149533
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  • 8. Ring chromosome 18 in a patient with multiple anomalies.
    Palmer CG, Fareed N, Merritt AD.
    J Med Genet; 1967 Jun; 4(2):117-23. PubMed ID: 5619991
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  • 12. [Abnormal C group chromosome in several members of the same family].
    Emerit I, Vernant P.
    Humangenetik; 1968 Jun; 6(4):326-34. PubMed ID: 5713618
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  • 15. [Anomaly of chromosomic structure (46,XX,17q+) in a polymalformed child].
    Walbaum R, Dupuis C, Dehaene P, Delmas-Marsalet Y.
    Ann Genet; 1968 Mar; 11(1):53-5. PubMed ID: 5301757
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  • 16. An inherited 1;G translocation.
    Ebbin AJ, Wilson MG, Towner JW, Forsman I.
    J Med Genet; 1971 Dec; 8(4):536-9. PubMed ID: 5149540
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  • 18. A profoundly mentally handicapped woman with a ring chromosome 22.
    Veall RM, Rundle AT, Chitham RC, Saldana-Garcia P.
    J Ment Defic Res; 1975 Dec; 19(3-4):225-43. PubMed ID: 1214291
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