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281 related items for PubMed ID: 11284430

  • 1. [Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].
    Balícek P, Jüttnerová V, Jarosová M, Fialová J, Fiedler Z, Kolmanová J.
    Cas Lek Cesk; 2001 Mar 01; 140(4):122-4. PubMed ID: 11284430
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  • 2. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
    Chen CP, Chern SR, Lee CC, Lin CC, Li YC, Hsieh LJ, Chen WL, Wang W.
    Prenat Diagn; 2006 Feb 01; 26(2):138-46. PubMed ID: 16470734
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  • 3. Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.
    Iqbal MA, Ramadan S, Ali FA, Kurdi W.
    Prenat Diagn; 2005 Dec 01; 25(12):1142-9. PubMed ID: 16240463
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  • 4. Prenatal diagnosis of an extra der(4) resulting from a complex maternal chromosome translocation.
    Migliori MV, Pettinari A, Ciaschini AM, Piermattei P, Pigliapoco F, Discepoli G.
    Prenat Diagn; 2004 Apr 01; 24(4):290-2. PubMed ID: 15065104
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  • 5. Molecular analysis by fluorescence in situ hybridization of a prenatally detected de novo complex chromosomal rearrangement t(2q;3p;4q;13q).
    Mercier S, Fellmann F, Cattin J, Bresson JL.
    Prenat Diagn; 1996 Nov 01; 16(11):1046-50. PubMed ID: 8953640
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  • 6. Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs.
    Giardino D, Corti C, Ballarati L, Finelli P, Valtorta C, Botta G, Giudici M, Grosso E, Larizza L.
    Prenat Diagn; 2006 Jun 01; 26(6):565-70. PubMed ID: 16683274
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  • 7. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
    Pires A, Ramos L, Venâncio M, Rei AI, Castedo S, Saraiva J.
    Prenat Diagn; 2005 Apr 01; 25(4):292-5. PubMed ID: 15849779
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  • 10. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
    Peschka B, Leygraaf J, Hansmann D, Hansmann M, Schröck E, Ried T, Engels H, Schwanitz G, Schubert R.
    Prenat Diagn; 1999 Dec 01; 19(12):1143-9. PubMed ID: 10590433
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  • 12. Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
    Chen CP, Chern SR, Wu PC, Tsai FJ, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2009 Dec 01; 48(4):389-99. PubMed ID: 20045761
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  • 13. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.
    Wang H, McLaughlin M, Thompson C, Hunter AG.
    Am J Med Genet; 1993 Jun 15; 46(5):559-62. PubMed ID: 8322821
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  • 14. 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 15; 25(6):451-5. PubMed ID: 15966060
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  • 15. Prenatally diagnosed de novo apparently balanced complex chromosome rearrangements: two new cases and review of the literature.
    Ruiz C, Grubs RE, Jewett T, Cox-Jones K, Abruzzese E, Pettenati MJ, Rao PN.
    Am J Med Genet; 1996 Aug 23; 64(3):478-84. PubMed ID: 8862625
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  • 16. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
    Ozkinay F, Kanit H, Onay H, Cogulu O, Gunduz C, Ercal D, Ozkinay C.
    Genet Couns; 2006 Aug 23; 17(3):315-20. PubMed ID: 17100200
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  • 17. Semilobar holoprosencephaly prenatal diagnosis: an unexpected complex rearrangement in a de novo apparently balanced reciprocal translocation on karyotype.
    Kanafani S, Aboura A, Pipiras E, Carbillon L, Tabet AC, Largillière C, Garel C, Gressens P, Bucourt M, Cedrin-Durnerin I, Lachassinne E, Roumegoux C, Uzan M, Hugues JN, Wolf JP, Benzacken B.
    Prenat Diagn; 2007 Mar 23; 27(3):279-84. PubMed ID: 17269127
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  • 19. Complex chromosomal rearrangement and intracytoplasmic sperm injection: a case report.
    Joly-Helas G, de La Rochebrochard C, Mousset-Siméon N, Moirot H, Tiercin C, Romana SP, Le Caignec C, Clavier B, Macé B, Rives N.
    Hum Reprod; 2007 May 23; 22(5):1292-7. PubMed ID: 17283038
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  • 20. 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 23; 22(11):957-61. PubMed ID: 12424755
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