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There are 16776 results for: content related to: Investigation of factors associated with paternal nondisjunction of chromosome 21

  1. Preconception folic acid supplementation and risk for chromosome 21 nondisjunction: A report from the National Down Syndrome Project

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 438–444, NaTasha D. Hollis, Emily G. Allen, Tiffany Renee Oliver, Stuart W. Tinker, Charlotte Druschel, Charlotte A. Hobbs, Leslie A. O'Leary, Paul A. Romitti, Marjorie H. Royle, Claudine P. Torfs, Sallie B. Freeman, Stephanie L. Sherman and Lora J.H. Bean

    Version of Record online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35796

  2. There are two mechanisms of achiasmate segregation in Drosophila females, one of which requires heterochromatic homology

    Developmental Genetics

    Volume 13, Issue 6, 1992, Pages: 440–467, R. Scott Hawley, Holly Irick, Deana A. Haddox, Michelle D. Whitley, Tamar Arbel, Janet Jang, Kim McKim, Anne E. Zitron, Christine New, Geoffrey Childs and Allan Lohe

    Version of Record online : 6 FEB 2005, DOI: 10.1002/dvg.1020130608

  3. Etiology of nondisjunction in humans

    Environmental and Molecular Mutagenesis

    Volume 25, Issue S2, 1995, Pages: 38–47, Michael A. Abruzzo and Terry J. Hassold

    Version of Record online : 14 JUL 2006, DOI: 10.1002/em.2850250608

  4. Nondisjunction

    Standard Article

    Encyclopedia of Genetics, Genomics, Proteomics and Bioinformatics

    Neil E. Lamb

    Published Online : 15 APR 2005, DOI: 10.1002/047001153X.g102307

  5. Parental age-related aneuploidy in human germ cells and offspring: A story of past and present

    Environmental and Molecular Mutagenesis

    Volume 28, Issue 3, 1996, Pages: 211–236, Ursula Eichenlaub-Ritter

    Version of Record online : 21 DEC 1998, DOI: 10.1002/(SICI)1098-2280(1996)28:3<211::AID-EM6>3.0.CO;2-G

  6. Down syndrome: genetic recombination and the origin of the extra chromosome 21

    Clinical Genetics

    Volume 57, Issue 2, February 2000, Pages: 95–100, Terry Hassold and Stephanie Sherman

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1399-0004.2000.570201.x

  7. The origin of trisomy 22: Evidence for acrocentric chromosome-specific patterns of nondisjunction

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 19, 1 October 2007, Pages: 2249–2255, Heather E. Hall, Urvashi Surti, Lori Hoffner, Sofia Shirley, Eleanor Feingold and Terry Hassold

    Version of Record online : 17 AUG 2007, DOI: 10.1002/ajmg.a.31918

  8. Origin of nondisjunction in trisomy 21 syndrome: All studies compiled, parental age analysis, and international comparisons

    American Journal of Medical Genetics

    Volume 16, Issue 1, September 1983, Pages: 111–116, Dr. Richard C. Juberg and Philip N. Mowrey

    Version of Record online : 3 JUN 2005, DOI: 10.1002/ajmg.1320160117

  9. Recurrent trisomy 21 in a couple with a child presenting trisomy 21 mosaicism and maternal uniparental disomy for chromosome 21 in the euploid cell line

    American Journal of Medical Genetics

    Volume 94, Issue 1, 4 September 2000, Pages: 35–41, Hélène Bruyère, Rosemarie Rupps, Brian D. Kuchinka, Jan M. Friedman and Wendy P. Robinson

    Version of Record online : 6 SEP 2000, DOI: 10.1002/1096-8628(20000904)94:1<35::AID-AJMG8>3.0.CO;2-9

  10. The origin of trisomy 13

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 19, 1 October 2007, Pages: 2242–2248, Heather E. Hall, E. Ricky Chan, Andrew Collins, LuAnn Judis, Sofia Shirley, Urvashi Surti, Lori Hoffner, Annette E. Cockwell, Patricia A. Jacobs and Terry J. Hassold

    Version of Record online : 12 SEP 2007, DOI: 10.1002/ajmg.a.31913

  11. High production of nondisjunction mutants in the offspring of Drosophila melanogaster females exposed to carbon dioxide at meiosis I

    Environmental and Molecular Mutagenesis

    Volume 31, Issue 2, 1998, Pages: 176–182, Kazuo Fujikawa, Masahiro Matsubara, Tetsuo Itoh and Sohei Kondo

    Version of Record online : 21 DEC 1998, DOI: 10.1002/(SICI)1098-2280(1998)31:2<176::AID-EM10>3.0.CO;2-9

  12. Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: A complex series of events

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 16, 15 August 2008, Pages: 2086–2093, Sophie Dahoun, Sarantis Gagos, Maryline Gagnebin, Corinne Gehrig, Carole Burgi, Fabienne Simon, Chantal Vieux, Philippe Extermann, Robert Lyle, Michael A. Morris, Stylianos E. Antonarakis, Frédérique Béna and Jean-Louis Blouin

    Version of Record online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32431

  13. You have free access to this content
    The Drosophila UBC9 homologue lesswright mediates the disjunction of homologues in meiosis I

    Genes to Cells

    Volume 6, Issue 3, March 2001, Pages: 215–224, Sergey Apionishev, Deepak Malhotra, Seshasayee Raghavachari, Soichi Tanda and Rebekah S. Rasooly

    Version of Record online : 7 JUL 2008, DOI: 10.1046/j.1365-2443.2001.00413.x

  14. Epidemiology of Down syndrome

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 13, Issue 3, 2007, Pages: 221–227, Stephanie L. Sherman, Emily G. Allen, Lora H. Bean and Sallie B. Freeman

    Version of Record online : 1 OCT 2007, DOI: 10.1002/mrdd.20157

  15. The Origin and Etiology of Trisomy 21

    Down Syndrome: Visions for the 21st Century

    Terry Hassold, Stephanie Sherman, Pages: 295–301, 2003

    Published Online : 21 MAR 2003, DOI: 10.1002/0471227579.ch21

  16. A semiselective test for the detection of first- and second-division nondisjunction in Drosophila melanogaster

    Environmental Mutagenesis

    Volume 8, Issue 2, 1986, Pages: 173–182, Dr. Polly A. Foureman

    Version of Record online : 14 JUL 2006, DOI: 10.1002/em.2860080202

  17. You have full text access to this Open Access content
    Relationship between effects of X-rays on nondisjunction and crossing over in Drosophila melanogaster

    Hereditas

    Volume 80, Issue 2, September 1975, Pages: 195–204, MARJA-LIISA SAVONTAUS

    Version of Record online : 12 FEB 2009, DOI: 10.1111/j.1601-5223.1975.tb01519.x

  18. You have free access to this content
    Human aneuploidy: lessons from achiasmate segregation in Drosophila melanogaster

    Annals of Human Genetics

    Volume 62, Issue 6, November 1998, Pages: 467–479, K. E. KOEHLER and T. J. HASSOLD

    Version of Record online : 5 MAR 2003, DOI: 10.1046/j.1469-1809.1998.6260467.x

  19. Saccharomyces cerevisiae mutants defective in chromosome segregation

    Yeast

    Volume 5, Issue 4, July/August 1989, Pages: 271–284, Jeffrey T. McGrew, Zhixiong Xiao and Molly Fitzgerald-Hayes

    Version of Record online : 29 JAN 2004, DOI: 10.1002/yea.320050407

  20. BrDU-Giemsa labeling studies of satellite associations in parents of children with trisomy 21 or 13

    American Journal of Medical Genetics

    Volume 26, Issue 4, April 1987, Pages: 971–981, Sandra Lee Gould, Dr. Patricia A. Martin-DeLeon and James F. Reynolds

    Version of Record online : 4 JUN 2005, DOI: 10.1002/ajmg.1320260428