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Journal Abstract Search

246 related items for PubMed ID: 15057955

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  • 2. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
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  • 7. Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
    Chen CP, Chern SR, Lee CC, Chen LF, Chin DT, Tzen CY, Wang W.
    Prenat Diagn; 2003 Sep; 23(9):758-61. PubMed ID: 12975789
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  • 8. Prenatal diagnosis of trisomy 3 mosaicism.
    Zaslav AL, Pierno G, Davis J, Fougner A, Jacob J, Kazi R, Blumenthal D, Sturim S, Shaham M, Fox J.
    Prenat Diagn; 2004 Sep; 24(9):693-6. PubMed ID: 15386452
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  • 9. Prenatal identification of a marker chromosome 16 by chromosome microdissection and reverse FISH.
    de Pater J, Van der Sijs-Bos C, Prins M, Derks J, Albrechts J, Engelen J.
    Eur J Med Genet; 2006 Sep; 49(4):306-12. PubMed ID: 16461028
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  • 11. Prenatal diagnosis of a fetus with pure partial trisomy 1q32-44 due to a familial balanced rearrangement.
    Kímya Y, Yakut T, Egelí U, Ozerkan K.
    Prenat Diagn; 2002 Nov; 22(11):957-61. PubMed ID: 12424755
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  • 12. Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.
    Prontera P, Buldrini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, Sensi A, Calzolari E, Donti E.
    Prenat Diagn; 2006 Jun; 26(6):571-6. PubMed ID: 16683276
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  • 13. M-FISH applications in clinical genetics.
    Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G.
    Genet Couns; 2005 Jun; 16(3):257-68. PubMed ID: 16259323
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  • 15. Prenatal diagnosis of a partial 6q trisomy: a case report.
    Valerio D, Di Domenico A, Felicetti M, La Boccetta A, Ferrara C, Antonio N, Borrelli AL.
    Prenat Diagn; 2006 Oct; 26(10):917-9. PubMed ID: 16845680
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  • 16. Prenatal diagnosis of trisomy 6 mosaicism.
    Destree A, Fourneau C, Dugauquier C, Rombout S, Sartenaer D, Gillerot Y.
    Prenat Diagn; 2005 May; 25(5):354-7. PubMed ID: 15906424
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  • 17. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
    Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.
    Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
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