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Journal Abstract Search

270 related items for PubMed ID: 1003448

  • 1. 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
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  • 2. Duplication-deficiency of chromosome 18, resulting from recombination of a paternal pericentric invesion, with a note for genetic counselling.
    Teyssier JR, Bajolle F.
    Hum Genet; 1980 Feb; 53(2):195-200. PubMed ID: 7358386
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  • 3. 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
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  • 5. [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
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  • 10. [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 Jun; 26(3):180-2. PubMed ID: 6606381
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  • 13. Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333).
    Beemer FA, de France HF, Rosina-Angelista IJ, Gerards LJ, Cats BP, Guyt R.
    Clin Genet; 1984 Sep; 26(3):209-15. PubMed ID: 6478641
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  • 16. [The partial deletion of the long arm of chromosome 18 (syndrome 18Q-). Report of two cases].
    Destiné ML, Punnett HH, Thovichit S, DiGeorge AM, Weiss L.
    Ann Genet; 1967 Jun; 10(2):65-9. PubMed ID: 5298975
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