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Journal Abstract Search

231 related items for PubMed ID: 1952786

  • 1. Branchial arch anomalies in trisomy 18.
    Verloes A, Seret N, Bernier V, Gonzales M, Herens C, Koulischer L.
    Ann Genet; 1991; 34(1):22-4. PubMed ID: 1952786
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  • 2. Unilateral microtia in an infant with trisomy 18 mosaicism.
    Giannatou E, Leze H, Katana A, Kolialexi A, Mavrou A, Kanavakis E, Kitsiou-Tzeli S.
    Genet Couns; 2009; 20(2):181-7. PubMed ID: 19650416
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  • 3. Microtia in infants with chromosomal trisomy.
    Zlotogora J, Eidelman A, Dudin A, Voss R.
    J Craniofac Genet Dev Biol; 1988; 8(3):205-6. PubMed ID: 3209683
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  • 4. [HELLP syndrome and trisomy 18 in a multi-parity patient].
    Mueller MD, Brühwiler H.
    Z Geburtshilfe Neonatol; 1996; 200(3):119-21. PubMed ID: 8963884
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  • 11. Trisomy 16p in a liveborn infant and review of trisomy 16p.
    O'Connor TA, Higgins RR.
    Am J Med Genet; 1992 Feb 01; 42(3):316-9. PubMed ID: 1536169
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  • 14. Fluorescence in situ hybridisation on formalin fixed fetal tissue in the diagnosis of chromosomal syndromes.
    Cobben JM, Essed CE, Hirdes J, Kraayenbrink RA, Van der Veen A.
    Genet Couns; 1994 Feb 01; 5(2):141-5. PubMed ID: 7917121
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  • 15. Further delineation of 7p trisomy. Case report and review of literature.
    Pallotta R, Dalprà L, Fusilli P, Zuffardi O.
    Ann Genet; 1996 Feb 01; 39(3):152-8. PubMed ID: 8839888
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  • 18. Trisomy 22 in a liveborn infant with multiple congenital anomalies.
    McPherson E, Stetka DG.
    Am J Med Genet; 1990 May 01; 36(1):11-4. PubMed ID: 2333899
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  • 19. Non-mosaic tetrasomy 9p in a liveborn infant with multiple congenital anomalies: case report and comparison with trisomy 9p.
    Leichtman LG, Zackowski JL, Storto PD, Newlin A.
    Am J Med Genet; 1996 Jun 14; 63(3):434-7. PubMed ID: 8737648
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  • 20. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
    Jalal SM, Martin JA, Benjamin TR, Kukolich MK, Townsend-Parcham JK.
    Ann Genet; 1990 Jun 14; 33(3):173-5. PubMed ID: 2288463
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