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Journal Abstract Search

457 related items for PubMed ID: 11391511

  • 1. [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; ; 32(8):746-50. PubMed ID: 11391511
    [Abstract] [Full Text] [Related]

  • 2. Ring chromosome 8 associated with microcephaly.
    Mingarelli R, Valorani G, Zelante L, Dallapiccola B.
    Ann Genet; 1991; 34(2):90-2. PubMed ID: 1746890
    [Abstract] [Full Text] [Related]

  • 3. Identification of supernumerary ring chromosome 1 mosaicism using fluorescence in situ hybridization.
    Chen H, Tuck-Muller CM, Batista DA, Wertelecki W.
    Am J Med Genet; 1995 Mar 27; 56(2):219-33. PubMed ID: 7625449
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  • 4. Effect of the size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrome: analysis of 13 patients with a de novo deletion.
    Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G.
    Eur J Hum Genet; 2000 Jul 27; 8(7):519-26. PubMed ID: 10909852
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  • 5. Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.
    Toriello HV, Higgins JV.
    Am J Med Genet; 1995 Jan 16; 55(2):200-4. PubMed ID: 7717418
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  • 6. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
    Kara N, Okten G, Guneş SO, Saglam Y, Tasdemir HA, Pinarli FA.
    Epilepsy Res; 2008 Aug 16; 80(2-3):219-23. PubMed ID: 18485670
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  • 7. 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 16; 35(2):269-73. PubMed ID: 2178418
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  • 8. Ring chromosome 7 in an Indian woman.
    Kaur A, Dhillon S, Garg PD, Singh JR.
    J Intellect Dev Disabil; 2008 Mar 16; 33(1):87-94. PubMed ID: 18300171
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  • 10. Ring chromosome 5 associated with severe growth retardation as the sole major physical abnormality.
    Migliori MV, Cherubini V, Bartolotta E, Pettinari A, Pecora R.
    Am J Med Genet; 1994 Jan 01; 49(1):108-10. PubMed ID: 8172236
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  • 12. Ring chromosome 22 resulting in partial monosomy in a mentally retarded boy.
    Gibbons B, Tan SY, Tam PY.
    Singapore Med J; 1999 Apr 01; 40(4):273-5. PubMed ID: 10487083
    [Abstract] [Full Text] [Related]

  • 13. Mental retardation and Ullrich-Turner syndrome in cases with 45,X/46X,+mar: additional support for the loss of the X-inactivation center hypothesis.
    Cole H, Huang B, Salbert BA, Brown J, Howard-Peebles PN, Black SH, Dorfmann A, Febles OR, Stevens CA, Jackson-Cook C.
    Am J Med Genet; 1994 Aug 15; 52(2):136-45. PubMed ID: 7801998
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  • 17. Interstitial deletion 2q33.3-q34 in a boy with a phenotype resembling the Seckel syndrome.
    Courtens W, Speleman F, Messiaen L, Bormans J, Van Roy N, Vamos E.
    Am J Med Genet; 1997 Sep 05; 71(4):479-85. PubMed ID: 9286460
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  • 19. De novo ring chromosome 6 in a child with multiple congenital anomalies.
    Ahzad HA, Ramli SF, Loong TM, Salahshourifar I, Zilfalil BA, Yusoff NM.
    Kobe J Med Sci; 2010 Sep 28; 56(2):E79-84. PubMed ID: 21063149
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  • 20. Clinical findings in an Arab boy with ring (14)(mos 46,XY,r(14)/45,XY,-14).
    Portoian-Shuhaiber S, Al-Awadi S, Farag TI, Sundareshan TS, Jindal HR, Al-Rashied AA.
    Ann Genet; 1986 Sep 28; 29(2):122-4. PubMed ID: 3490208
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