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PUBMED FOR HANDHELDS

Journal Abstract Search


347 related items for PubMed ID: 5306712

  • 1. A ring chromosome (46,XY,13r) occurring in a family with a D-D translocation 13-,14-, t(13q 14q).
    Mikkelsen M, Niebuhr E.
    Ann Genet; 1969 Mar; 12(1):51-6. PubMed ID: 5306712
    [No Abstract] [Full Text] [Related]

  • 2. Familial translocation between chromosomes of groups C and D (46, T(Cq-;Dq+).
    Tal'vik TA, Mikel'saar AV, Mikel'saar RV.
    Sov Genet; 1974 Jun 01; 8(5):651-7. PubMed ID: 4413436
    [No Abstract] [Full Text] [Related]

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  • 4. [The Dr phenotype: a study of threee cases with a ring D chromosome].
    Lejeune J, Lafourcade J, Berger R, Cruveiller J, Rethoré MO, Dutrillaux B, Abonyi D, Jérôme H.
    Ann Genet; 1968 Jun 01; 11(2):79-87. PubMed ID: 5303427
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  • 8. [A case of translocation t(Cp-; Bp+)].
    Ricci N, Ventimiglia B, Dallapiccola B, Preto G.
    Ann Genet; 1967 Jun 01; 10(2):82-5. PubMed ID: 5298977
    [No Abstract] [Full Text] [Related]

  • 9. [Ring chromosome 18].
    Ricci N, Dallapiccola B, Ventimiglia B, Preto G.
    Acta Genet Med Gemellol (Roma); 1970 Jul 01; 19(3):439-47. PubMed ID: 5495679
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  • 11. Chromosomal aberration involving a member of the D group in a mentally retarded child with multiple congenital anomalies.
    Giorgi PL, Paci A, Ceccarelli M, Vizzoni L.
    Helv Paediatr Acta; 1967 Oct 01; 22(5):466-71. PubMed ID: 5595749
    [No Abstract] [Full Text] [Related]

  • 12. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov 01; 15(5):469-73. PubMed ID: 7332149
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  • 13. [Abnormal C group chromosome in several members of the same family].
    Emerit I, Vernant P.
    Humangenetik; 1968 Nov 01; 6(4):326-34. PubMed ID: 5713618
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  • 14. Aberrant serum protein inheritance in a patient with a ring D chromosome.
    Daniel WL.
    Pediatrics; 1970 Jul 01; 46(1):120-3. PubMed ID: 5423439
    [No Abstract] [Full Text] [Related]

  • 15. [A new case of a ring shaped chromosome 18 (18 r)].
    Petit P, Poncelet R.
    Ann Genet; 1967 Sep 01; 10(3):134-7. PubMed ID: 5300397
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  • 19. Partial trisomy 9 in the case of familial translocation 8/9 mat.
    Schwanitz G, Schamberger U, Rott HD, Wieczorek V.
    Ann Genet; 1974 Sep 01; 17(3):163-6. PubMed ID: 4548816
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  • 20. Inherited translocations in two families (t(14q+;10q-) and t(13q-;21q+)).
    Talvik T, Mikelsaar AV, Mikelsaar R, Käosaar M, Tüür S.
    Humangenetik; 1973 Sep 20; 19(3):215-26. PubMed ID: 4763926
    [No Abstract] [Full Text] [Related]


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