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Journal Abstract Search

397 related items for PubMed ID: 8172236

  • 1. 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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  • 8. [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; 1994 Jan 01; 32(8):746-50. PubMed ID: 11391511
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  • 11. Ring chromosome 22 and autism: report and review.
    MacLean JE, Teshima IE, Szatmari P, Nowaczyk MJ.
    Am J Med Genet; 2000 Feb 28; 90(5):382-5. PubMed ID: 10706359
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  • 12. Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.
    de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B, Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP.
    Am J Med Genet; 1995 Nov 20; 59(3):369-74. PubMed ID: 8599364
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  • 13. 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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  • 18. Interstitial deletion and ring chromosome derived from 19q. Proximal 19q trisomy phenotype.
    Quack B, Van Roy N, Verschraegen-Spae MR, Klein F.
    Ann Genet; 1992 Mar 27; 35(4):241-4. PubMed ID: 1296524
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