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Journal Abstract Search

151 related items for PubMed ID: 317785

  • 1. Some clinical and cytogenetic observations on a ring chromosome 13 (p11 q34).
    Hernandez A, Garcia-Cruz D, Plascencia L, Nazara Z, Rivera H, Sanchez-Corona J, Cantu JM.
    Ann Genet; 1979; 22(4):221-4. PubMed ID: 317785
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  • 2. [Ring chromosome 13 and multiple malformations (author's transl)].
    Antich J, Plaza J, Geán E.
    An Esp Pediatr; 1981 Nov; 15(5):469-73. PubMed ID: 7332149
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  • 7. Ring chromosome 2 in a child with growth failure and few congenital abnormalities.
    Vigfusson NV, Kapstafer KJ, Lloyd MA.
    Am J Med Genet; 1980 Nov; 7(3):383-9. PubMed ID: 7468662
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  • 8. Isochromosome-formation in chromosome 9.
    Miller K, Arslan-Kirchner M.
    Ann Genet; 1994 Nov; 37(2):78-81. PubMed ID: 7985983
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  • 9. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R, Paolieri M, Anichini C, Scarinci R, Berardi R, Rosaia L, Pucci L.
    Boll Soc Ital Biol Sper; 1992 Apr; 68(4):263-9. PubMed ID: 1463601
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  • 14. Aberrant serum protein inheritance in a patient with a ring D chromosome.
    Daniel WL.
    Pediatrics; 1970 Jul; 46(1):120-3. PubMed ID: 5423439
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  • 16. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
    Su PH, Chen CP, Su YN, Chen SJ, Lin LL, Chen JY.
    Genet Mol Res; 2013 Apr 25; 12(2):1311-7. PubMed ID: 23661454
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  • 17. Partial trisomy 15 in a male with severe psychomotor retardation (48, XY, + 15q -, + mar(15)).
    Voss R, Lerer I, Maftzir G, Sheinis M, Cohen MM.
    Am J Med Genet; 1982 Jun 25; 12(2):131-9. PubMed ID: 7102721
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  • 20. 46,X,i(Xq)/47,XX,+13 mosaicism.
    Igarashi M, Tsukahara M, Sugio Y, Katayama K, Kajii T.
    Ann Genet; 1985 Jun 25; 28(4):241-4. PubMed ID: 3879438
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