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    Results: 1 to 20 of 157

    1.

    Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature.

    Vorsanova SG, Iourov IY, Voinova-Ulas VY, Weise A, Monakhov VV, Kolotii AD, Soloviev IV, Novikov PV, Yurov YB, Liehr T.

    Mol Cytogenet. 2008 Jun 19;1:13.PMID: 18564437 [PubMed - in process]Free PMC ArticleFree textRelated citations

    2.

    De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21.

    Riegel M, Baumer A, Piram A, Ortolan D, Peres LC, Pina-Neto JM.

    Genet Couns. 2001;12(1):69-75.PMID: 11332980 [PubMed - indexed for MEDLINE]Related citations

    3.

    A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18.

    Quadrelli R, Quadrelli A, Milunsky A, Zou YS, Huang XL, Viera E, Mechoso B, Bellini S, Costabel M, Vaglio A.

    Genet Test Mol Biomarkers. 2009 Jun;13(3):387-93.PMID: 19473082 [PubMed - indexed for MEDLINE]Related citations

    4.

    Application of molecular and cytogenetic techniques to the detection of a de novo unbalanced t(11q;21q) in a patient previously diagnosed as having monosomy 21.

    Hertz B, Brandt CA, Petersen MB, Pedersen S, König U, Strømkjaer H, Jensen PK.

    Clin Genet. 1993 Aug;44(2):89-94.PMID: 7506129 [PubMed - indexed for MEDLINE]Related citations

    5.

    Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.

    Petković I, Barisić I, Bastić M, Hećimović S, Bago R.

    Am J Med Genet A. 2003 Jul 15;120A(2):266-71.PMID: 12833412 [PubMed - indexed for MEDLINE]Related citations

    6.

    Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).

    Chen CP, Lin SP, Lin CC, Li YC, Chern SR, Chen WM, Lee CC, Hsieh LJ, Wang W.

    Prenat Diagn. 2005 Feb;25(2):112-8. Review.PMID: 15712324 [PubMed - indexed for MEDLINE]Related citations

    7.

    Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.

    McGhee EM, Qu Y, Wohlferd MM, Goldberg JD, Norton ME, Cotter PD.

    Clin Genet. 2001 Apr;59(4):274-8.PMID: 11298684 [PubMed - indexed for MEDLINE]Related citations

    8.

    Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21.

    Riegel M, Hargreaves P, Baumer A, Guc-Scekic M, Ignjatovic M, Schinzel A.

    Eur J Med Genet. 2005 Apr-Jun;48(2):167-74. Epub 2005 Feb 17.PMID: 16053908 [PubMed - indexed for MEDLINE]Related citations

    9.

    A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].

    Grasshoff U, Singer S, Liehr T, Starke H, Fode B, Schöning M, Dufke A.

    Cytogenet Genome Res. 2003;103(1-2):17-23. Erratum in: Cytogenet Genome Res. 2004;105(1):160. PMID: 15004458 [PubMed - indexed for MEDLINE]Related citations

    10.

    Monosomy for 21pter-q21: case report and assignment of a DNA clone (Fr8-77) to the deleted segment.

    Abe K, Deng HX, Harada N, Yoshiura K, Oh-Hira T, Niikawa N.

    Jinrui Idengaku Zasshi. 1990 Dec;35(4):303-10.PMID: 2094779 [PubMed - indexed for MEDLINE]Related citations

    11.

    Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.

    Alkan M, Ramelli GP, Hirsiger H, Keser I, Remonda L, Bühler EM, Moser H.

    Genet Couns. 2002;13(2):151-6.PMID: 12150215 [PubMed - indexed for MEDLINE]Related citations

    12.

    Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report.

    Ahn JM, Koo DH, Kwon KW, Lee YK, Lee YH, Lee HH, Nam KH, Lee KH.

    J Korean Med Sci. 2003 Feb;18(1):112-3.PMID: 12589098 [PubMed - indexed for MEDLINE]Free ArticleRelated citations

    13.

    A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).

    Balci S, Aypar E, Beksaç MS, Bartsch O.

    Genet Couns. 2009;20(2):125-32.PMID: 19650409 [PubMed - indexed for MEDLINE]Related citations

    14.

    Partial trisomy of the distal part of 10q: a report of two Egyptian cases.

    Aglan MS, Kamel AK, Helmy NA.

    Genet Couns. 2008;19(2):199-209.PMID: 18618995 [PubMed - indexed for MEDLINE]Related citations

    15.

    Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.

    Chen CP, Lin CC, Li YC, Hsieh LJ, Lee CC, Wang W.

    Fertil Steril. 2006 Nov;86(5):1514.e1-2.PMID: 17070202 [PubMed - indexed for MEDLINE]Related citations

    16.

    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. Review.PMID: 16506269 [PubMed - indexed for MEDLINE]Related citations

    17.

    Cytogenetic and molecular studies of an X;21 translocation previously diagnosed as complete monosomy 21.

    Cardoso LC, Moraes L, Camilo MJ, Mulatinho MV, Ramos H, Almeida JC, Llerena JC Jr, Seuánez HN, Vargas FR.

    Eur J Med Genet. 2008 Nov-Dec;51(6):588-97. Epub 2008 Jul 12.PMID: 18674646 [PubMed - indexed for MEDLINE]Related citations

    18.

    Recessive cancer genes in meningiomas? An analysis of 31 cases.

    Casalone R, Granata P, Simi P, Tarantino E, Butti G, Buonaguidi R, Faggionato F, Knerich R, Solero L.

    Cancer Genet Cytogenet. 1987 Jul;27(1):145-59.PMID: 3472644 [PubMed - indexed for MEDLINE]Related citations

    19.

    Mosaic trisomy 21/monosomy 21 in a living female infant.

    Nguyen HP, Riess A, Krüger M, Bauer P, Singer S, Schneider M, Enders H, Dufke A.

    Cytogenet Genome Res. 2009;125(1):26-32. Epub 2009 Jul 14.PMID: 19617693 [PubMed - indexed for MEDLINE]Related citations

    20.

    Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-qter/ monosomy 9p23-pter.

    Cohn AC, Kearns LS, Savarirayan R, Ryan J, Craig JE, Mackey DA.

    Ophthalmic Genet. 2005 Mar;26(1):45-53. Review.PMID: 15823925 [PubMed - indexed for MEDLINE]Related citations

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