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Journal Abstract Search

190 related items for PubMed ID: 9160390

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  • 25. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W.
    Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
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  • 28. Exclusion of uniparental inheritance of chromosome 15 in a fetus with a familial dicentric (Y;15) translocation.
    White LM, Treat K, Leff A, Styers D, Mitchell M, Knoll JH.
    Prenat Diagn; 1998 Feb; 18(2):111-6. PubMed ID: 9516010
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  • 30. [Simultaneous presence of ins (15;17),t(2;17;20) and trisomy 8 in a patient with acute promyelocytic leukemia].
    Bai S, Xue Y, Wu Y, Pan J, Zhang J, Shen J, Wang Y, Qiu H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Dec; 25(6):712-4. PubMed ID: 19065540
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  • 35. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
    Coêlho KE, Egashira M, Kato R, Fujimoto M, Matsumoto N, Rerkamnuaychoke B, Abe K, Harada N, Ohashi H, Fukushima Y, Niikawa N.
    Am J Med Genet; 1996 Jun 14; 63(3):468-71. PubMed ID: 8737654
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  • 36. Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).
    Liehr T, Heller A, Eichhorn KH, Beensen V, Schulze E, Starke H, Claussen U, Schreyer I.
    Prenat Diagn; 2004 Dec 15; 24(12):1022-4. PubMed ID: 15614895
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  • 37. Chromosomal cryptic insertion of the terminal region and its formative mechanism determined by fluorescence in situ hybridization.
    Tan Y, Lu G.
    Chin Med J (Engl); 2002 Jul 15; 115(7):1039-42. PubMed ID: 12150739
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  • 39. Prenatally detected marker chromosome identified as an i(22)(p10) using (micro)FISH.
    Engelen JJ, Tuerlings JH, Albrechts JC, Schrander-Stumpel CT, Hamers AJ, De Die-Smulders CE.
    Genet Couns; 2000 Jul 15; 11(1):13-7. PubMed ID: 10756422
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