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There are 24758 results for: content related to: Familial translocation t(3;10) (p26.3;p12.31) leading to trisomy 10p12.31 [RIGHTWARDS ARROW] pter and monosomy 3p26.3 [RIGHTWARDS ARROW] pter in seven members

  1. Segregation of a t(1;3) translocation in multiple affected family members with both types of adjacent-1 segregants

    American Journal of Medical Genetics Part A

    Volume 124A, Issue 2, 15 January 2004, Pages: 118–128, Chahira Kozma, Anne M. Slavotinek and Jeanne M. Meck

    Version of Record online : 16 JUN 2003, DOI: 10.1002/ajmg.a.20332

  2. Severe musculoskeletal phenotype associated with an unbalanced t(6;10) translocation: Clarification of the locus for this phenotype on distal 6p

    American Journal of Medical Genetics Part A

    Volume 119A, Issue 3, 15 June 2003, Pages: 288–292, Paul A. James, Salim Aftimos and Paul Oei

    Version of Record online : 2 APR 2003, DOI: 10.1002/ajmg.a.20079

  3. Prenatal diagnosis and molecular cytogenetics in a case of partial trisomy 14 and monosomy 21

    American Journal of Medical Genetics

    Volume 100, Issue 3, 1 May 2001, Pages: 246–250, Charles Lee, Darren J. Fowler, Emmanuelle Lemyre, Mary McH. Sandstrom, Lewis B. Holmes and Cynthia C. Morton

    Version of Record online : 2 MAY 2001, DOI: 10.1002/1096-8628(20010501)100:3<246::AID-AJMG1254>3.0.CO;2-N

  4. You have free access to this content
    Many unbalanced translocations show duplication of a translocation participant. Clinical and cytogenetic implications in myeloid hematologic malignancies

    American Journal of Hematology

    Volume 64, Issue 3, July 2000, Pages: 161–169, Bent Pedersen, Jan M. Nørgaard, Bjarne Bach Pedersen, Niels Clausen, Inge Helleberg Rasmussen and Karen Thorling

    Version of Record online : 15 JUN 2000, DOI: 10.1002/1096-8652(200007)64:3<161::AID-AJH4>3.0.CO;2-Q

  5. Cytogenetic abnormalities and clinical outcome in Wilms tumor: A study by the U.K. cancer cytogenetics group and the U.K. Children's Cancer Study Group

    Medical and Pediatric Oncology

    Volume 38, Issue 1, January 2002, Pages: 11–21, Nick Bown, Simon J. Cotterill, Paul Roberts, Mike Griffiths, Simon Larkins, Steve Hibbert, Helen Middleton, Anna Kelsey, Denise Tritton and Chris Mitchell

    Version of Record online : 21 DEC 2001, DOI: 10.1002/mpo.1258

  6. Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: Further delineation of partial trisomy 1q syndrome

    American Journal of Medical Genetics

    Volume 104, Issue 4, 15 December 2001, Pages: 312–318, Werner Emberger, E. Petek, P. M. Kroisel, H. Zierler and K. Wagner

    Version of Record online : 23 OCT 2001, DOI: 10.1002/ajmg.10096

  7. Omphalocele in trisomy 3q: further delineation of phenotype

    Clinical Genetics

    Volume 64, Issue 5, November 2003, Pages: 404–413, SA Yatsenko, R Mendoza-Londono, JW Belmont and LG Shaffer

    Version of Record online : 21 OCT 2003, DOI: 10.1034/j.1399-0004.2003.00159.x

  8. Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf–Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith–Wiedemann or Russell–Silver phenotype

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 20, 15 October 2008, Pages: 2691–2697, Sarah T. South, Heidi Whitby, Teresa Maxwell, Emily Aston, Arthur R. Brothman and John C. Carey

    Version of Record online : 16 SEP 2008, DOI: 10.1002/ajmg.a.32516

  9. Larsen-like phenotype associated with partial trisomy 3p and monosomy 5p

    Prenatal Diagnosis

    Volume 28, Issue 2, February 2008, Pages: 131–134, C. Goumy, A. M. Beaufrère, A. Tchirkov, L. Gouas, F. Gaspard, M. Giollant, T. Roucaute, L. Veronèse, D. Lemery and P. Vago

    Version of Record online : 30 JAN 2008, DOI: 10.1002/pd.1928

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    Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study

    Ultrasound in Obstetrics & Gynecology

    Volume 41, Issue 3, March 2013, Pages: 267–273, M. Schmid, S. Stary, S. Springer, D. Bettelheim, P. Husslein and B. Streubel

    Version of Record online : 4 MAR 2013, DOI: 10.1002/uog.12389

  11. Nuchal translucency thickness in the prediction of unbalanced translocations

    Prenatal Diagnosis

    Volume 34, Issue 10, October 2014, Pages: 982–985, Marta Arigita, Maribel Grande, Raquel Mula, Virginia Borobio, Aurora Sanchez, Anna Soler and Antoni Borrell

    Version of Record online : 11 JUN 2014, DOI: 10.1002/pd.4409

  12. A cryptic unbalanced translocation resulting in del 13q and dup 15q

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 19, 1 October 2008, Pages: 2570–2573, Alexandra Tészás, Rikke S. Møller, Richard Kellermayer, Márta Czakó, Klaus W. Kjaer, Reinhard Ullmann, Béla Melegh, Niels Tommerup and György Kosztolányi

    Version of Record online : 15 SEP 2008, DOI: 10.1002/ajmg.a.32394

  13. Unbalanced translocation (3;5)(q26.1;p14): A clinical report

    American Journal of Medical Genetics

    Volume 110, Issue 4, 15 July 2002, Pages: 353–358, Massimiliano Rossi, Pasqua Di Micco, Lucia Perone, Daniele De Brasi, Vito Guzzetta, Maria Vittoria Andreucci, Giovanna Roberta Vega, Maria Grazia Marzano, Emilia Iaccarino and Generoso Andria

    Version of Record online : 8 MAY 2002, DOI: 10.1002/ajmg.10440

  14. Trisomy 4 pter-q12 and monosomy of chromosome 13 pter-q12 in a male with deficiency of all blood lymphocyte populations

    American Journal of Medical Genetics

    Volume 102, Issue 2, 1 August 2001, Pages: 139–145, GopalRao V.N. Velagaleti, Lillian H. Lockhart, Frank C. Schmalstieg and Armond S. Goldman

    Version of Record online : 20 JUN 2001, DOI: 10.1002/ajmg.1444

  15. Prenatal diagnosis of partial trisomy 1q and monosomy X in a fetus with a congenital lung lesion and hydrops fetalis

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 10, 15 May 2007, Pages: 1104–1107, Tracy L. Pressey, R. Douglas Wilson, Stefanie Kasperski, Michael W. Bebbington and N. Scott Adzick

    Version of Record online : 12 APR 2007, DOI: 10.1002/ajmg.a.31707

  16. Molecular characterization of a patient with 3p deletion syndrome and a review of the literature

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 21, 1 November 2008, Pages: 2746–2752, Thomas V. Fernandez, I.J. García-González, Christopher E. Mason, G. Hernández-Zaragoza, V.C. Ledezma-Rodríguez, V.M. Anguiano-Alvarez, R. E'Vega, M. Gutiérrez-Angulo, M.L. Maya, H.E. García-Bejarano, M. González-Cruz, S. Barrios, R. Atorga, M.G. López-Cardona, J. Armendariz-Borunda, Matthew W. State and Nory O. Dávalos

    Version of Record online : 3 OCT 2008, DOI: 10.1002/ajmg.a.32533

  17. Congenital diaphragmatic hernia associated with duplication of 11q23-qter

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 14, 15 July 2006, Pages: 1580–1586, M. Klaassens, D.A. Scott, M. van Dooren, R. Hochstenbach, H.J. Eussen, W.W. Cai, R.J. Galjaard, C. Wouters, M. Poot, J. Laudy, B. Lee, D. Tibboel and A. de Klein

    Version of Record online : 12 JUN 2006, DOI: 10.1002/ajmg.a.31321

  18. Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13)

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 21, 1 November 2008, Pages: 2777–2784, Marzena Gajecka, Reem Saadeh, Katherine L. Mackay, Caron D. Glotzbach, Krystyna Spodar, David Chitayat and Lisa G. Shaffer

    Version of Record online : 27 OCT 2008, DOI: 10.1002/ajmg.a.32427

  19. Attenuated phenotype in a child with trisomy for 1q due to unbalanced X;1 translocation [46,X,der(X),t(X;1)(q28;q32.1)]

    American Journal of Medical Genetics Part A

    Volume 128A, Issue 1, 1 July 2004, Pages: 72–77, Svetlana A. Yatsenko, Trilochan Sahoo, Melinda Rosenkranz, Roberto Mendoza-Londono, Rizwan Naeem and Fernando Scaglia

    Version of Record online : 22 MAR 2004, DOI: 10.1002/ajmg.a.30094

  20. Unbalanced translocation in an adult patient with premature ovarian failure and mental retardation detected by spectral karyotyping and array-comparative genomic hybridization

    European Journal of Clinical Investigation

    Volume 39, Issue 8, August 2009, Pages: 729–737, Q. S. Guo, S. Y. Qin, S. F. Zhou, L. He, D. Ma, Y. P. Zhang, Y. Xiong, T. Peng, Y. Cheng and X. T. Li

    Version of Record online : 8 JUN 2009, DOI: 10.1111/j.1365-2362.2009.02141.x

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    Corrigendum

    Vol. 39, Issue 12, 1114, Version of Record online: 9 NOV 2009