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Journal Abstract Search

221 related items for PubMed ID: 2178418

  • 1. Loss of the 3p25.3 band is critical in the manifestation of del(3p) syndrome: karyotype-phenotype correlation in cases with deficiency of the distal portion of the short arm of chromosome 3.
    Narahara K, Kikkawa K, Murakami M, Hiramoto K, Namba H, Tsuji K, Yokoyama Y, Kimoto H.
    Am J Med Genet; 1990 Feb; 35(2):269-73. PubMed ID: 2178418
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  • 3. Clinical and molecular analyses of deletion 3p25-pter syndrome.
    Mowrey PN, Chorney MJ, Venditti CP, Latif F, Modi WS, Lerman MI, Zbar B, Robins DB, Rogan PK, Ladda RL.
    Am J Med Genet; 1993 Jul 01; 46(6):623-9. PubMed ID: 8103286
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  • 4. Molecular cytogenetic characterization of a subtle interstitial del(3)(p25.3p26.2) in a patient with deletion 3p syndrome.
    Cargile CB, Goh DL, Goodman BK, Chen XN, Korenberg JR, Semenza GL, Thomas GH.
    Am J Med Genet; 2002 Apr 22; 109(2):133-8. PubMed ID: 11977162
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  • 5. Complex translocation among chromosomes 2, 3, 9, 15, 18, 20 in a patient with 3p-syndrome.
    Omrani MD, Saleh Gargari S, Azizi F, Safavi Naini N, Omrani S.
    Arch Iran Med; 2014 Jul 22; 17(7):521-2. PubMed ID: 24979567
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  • 6. [Ring chromosome 8: microcephaly, mental retardation and minor facial anomalies with adhesive behavioral phenotype].
    Bibas Bonet H, Fontenla M, Fauze R, G de Pinat I.
    Rev Neurol; 2014 Jul 22; 32(8):746-50. PubMed ID: 11391511
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  • 7. Mother and son with deletion of 3p25-pter.
    Tazelaar J, Roberson J, Van Dyke DL, Babu VR, Weiss L.
    Am J Med Genet; 1991 May 01; 39(2):130-2. PubMed ID: 2063913
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  • 8. Deletion of the distal long arm of chromosome 1: a definable syndrome.
    Johnson VP, Heck LJ, Carter GA, Flom JO.
    Am J Med Genet; 1985 Dec 01; 22(4):685-94. PubMed ID: 4073121
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  • 13. Partial 1p monosomy in a physically and mentally retarded boy.
    Gencík A, Gencíkova A.
    J Genet Hum; 1987 Aug 01; 35(4):309-15. PubMed ID: 2958604
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  • 16. Ring chromosome 8 associated with microcephaly.
    Mingarelli R, Valorani G, Zelante L, Dallapiccola B.
    Ann Genet; 1991 Aug 01; 34(2):90-2. PubMed ID: 1746890
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  • 17. Interstitial deletion of long arm of chromosome 13.
    Carnevale A, Frias S, Alcantar R.
    Ann Genet; 1984 Aug 01; 27(1):49-52. PubMed ID: 6609673
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