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Journal Abstract Search

136 related items for PubMed ID: 3221208

  • 1. Familial trisomy 11p resulting from a balanced paternal translocation: 3 new cases including first trimester diagnosis.
    Ogur G, Hayez F, Herinckx A, Van Regemorter N, Vamos E.
    J Genet Hum; 1988 Aug; 36(4):323-9. PubMed ID: 3221208
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  • 2. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
    Tüysüz B, Hacihanefioglu S, Silahtaroglu A, Yilmaz S, Deviren A, Cenani A.
    Genet Couns; 2000 Aug; 11(4):355-61. PubMed ID: 11140413
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  • 3. Non-mosaic trisomy 16 in a third-trimester fetus.
    Yancey MK, Hardin EL, Pacheco C, Kuslich CD, Donlon TA.
    Obstet Gynecol; 1996 May; 87(5 Pt 2):856-60. PubMed ID: 8677115
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  • 4. Partial trisomy 11p with interatrial septal aneurysm. Case report and literature review.
    Aleck K, Williams J, Mongkolsmai C, Knight S, Taysi K.
    Ann Genet; 1985 May; 28(2):102-6. PubMed ID: 3876056
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  • 5. [Non-immunologic hydrops fetalis (NIHF)--case report of double partial trisomy 15q and 17q resulting from familial translocation 15/17 and cytogenetic findings in 50 cases with hydrops fetalis].
    Schmid G, Haverkamp F, Rechmann J, Schwanitz G, Zerres K, Hansmann M, Kowalewski S.
    Klin Padiatr; 1987 May; 199(4):309-14. PubMed ID: 3657040
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  • 6. 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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  • 7. [Familial balanced chromosome translocation t(12;13) in a family with several deformed stillbirths].
    Bommer C, Körner H.
    Zentralbl Gynakol; 1982 Nov; 104(24):1578-83. PubMed ID: 6892078
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  • 8. Prenatal diagnosis of partial trisomy 12q: clinical presentations and outcome.
    Peng HH, Wang TH, Hsueh DW, Chang SD, Soong YK.
    Prenat Diagn; 2005 Jun; 25(6):470-4. PubMed ID: 15966037
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  • 9. Prenatal diagnosis of a satellited non-acrocentric chromosome derived from a maternal translocation (10;13)(p13;p12) and review of literature.
    Faivre L, Morichon-Delvallez N, Viot G, Larget-Piet A, Narcy F, Turleau C, Pinson MP, Dumez Y, Munnich A, Vekemans M.
    Prenat Diagn; 1999 Mar; 19(3):282-6. PubMed ID: 10210132
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  • 10. A partial trisomy 15q due to 15;17 translocation detected by conventional cytogenetic and FISH techniques.
    Cora T, Acar H, Oran B.
    Genet Couns; 2000 Mar; 11(1):25-32. PubMed ID: 10756424
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  • 11. Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.
    Hacihanefioğlu S, Güven GS, Deviren A, Silahtaroğlu AN, Yosunvkaya Fenerci E, Ozkiliç A, Yüksel A.
    Genet Couns; 2002 Mar; 13(1):41-8. PubMed ID: 12017237
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 13. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages.
    Demirhan O, Tastemir D.
    Fertil Steril; 2006 Jul; 86(1):219.e15-9. PubMed ID: 16818035
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  • 18. Cryptic 1p36.3/6q25.2 translocation in three generations ascertained through a foetus with IUGR and cerebral malformations.
    Cavani S, Perfumo C, Faravelli F, Malacarne M, Sogliani M, Piombo G, Zerega G, Zucca M, Dagna Bricarelli F, Pierluigi M.
    Prenat Diagn; 2003 Oct; 23(10):819-23. PubMed ID: 14558026
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