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There are 272062 results for: content related to: X

  1. X

    Dictionary of DNA and Genome Technology

    Paul Singleton, Page: 283, 2008

    Published Online : 16 APR 2008, DOI: 10.1002/9780470696217.ch24

  2. Inheritance of most X-linked traits is not dominant or recessive, just X-linked

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 2, 30 August 2004, Pages: 136–143, William B. Dobyns, Allison Filauro, Brett N. Tomson, April S. Chan, Allen W. Ho, Nicholas T. Ting, Jan C. Oosterwijk and Carole Ober

    Article first published online : 29 JUN 2004, DOI: 10.1002/ajmg.a.30123

  3. Skewed X inactivation in healthy individuals and in different diseases

    Acta Paediatrica

    Volume 95, Issue S451, April 2006, Pages: 24–29, Karen Helene Ørstavik

    Article first published online : 2 JAN 2007, DOI: 10.1111/j.1651-2227.2006.tb02385.x

  4. Extracutaneous analogies of Blaschko lines

    American Journal of Medical Genetics

    Volume 85, Issue 4, 6 August 1999, Pages: 338–341, Hans-Dieter Rott

    Article first published online : 8 JUL 1999, DOI: 10.1002/(SICI)1096-8628(19990806)85:4<338::AID-AJMG5>3.0.CO;2-8

  5. Cutaneous clues for diagnosing X-chromosomal disorders

    Clinical Genetics

    Volume 85, Issue 4, April 2014, Pages: 328–335, M. Vreeburg, S.C.E.H. Sallevelt, A.P.A. Stegmann, M. van Geel, Y.J.H.A. Detisch, C.T.R.M. Schrander-Stumpel, M.A.M. van Steensel and D. Marcus-Soekarman

    Article first published online : 14 AUG 2013, DOI: 10.1111/cge.12162

  6. Clinical correlate: Tooth Agenesis

    Mineralized Tissues in Oral and Craniofacial Science

    Rena N. D'Souza, Gabriele I. Mues, Pages: 129–134, 2013

    Published Online : 5 APR 2013, DOI: 10.1002/9781118704868.ch15

  7. Case 27

    Practical Flow Cytometry in Haematology Diagnosis: 100 Worked Examples

    Mike Leach, Mark Drummond, Allyson Doig, Pam McKay, Bob Jackson, Barbara J. Bain, Pages: 93–94, 2015

    Published Online : 26 JUN 2015, DOI: 10.1002/9781118746950.ch27

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    Phenotype–genotype correlations in hemophilia A carriers are consistent with the binary role of the phase between F8 and X-chromosome inactivation

    Journal of Thrombosis and Haemostasis

    Volume 13, Issue 4, April 2015, Pages: 530–539, C. P. Radic, L. C. Rossetti, M. M. Abelleyro, T. Tetzlaff, M. Candela, D. Neme, G. Sciuccati, M. Bonduel, E. Medina-Acosta, I. B. Larripa, M. de Tezanos Pinto and C. D. De Brasi

    Article first published online : 14 MAR 2015, DOI: 10.1111/jth.12854

  9. Androgen Insensitivity Syndrome

    Standard Article

    The International Encyclopedia of Human Sexuality

    Liuhong Cai

    Published Online : 20 APR 2015, DOI: 10.1002/9781118896877.wbiehs028

  10. Mendelian Inheritance

    Prenatal Diagnosis: Cases & Clinical Challenges

    Miriam S. DiMaio, Joyce E. Fox, Maurice J. Mahoney, Pages: 22–65, 2010

    Published Online : 22 JUN 2010, DOI: 10.1002/9780470696262.ch2

  11. X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between Xq21.33 and Xq23

    American Journal of Medical Genetics

    Volume 85, Issue 3, 30 July 1999, Pages: 255–262, Albert E. Chudley, D.C. Tackels, Herbert A. Lubs, J. Fernando Arena, Wendi P. Stoeber, Sylvia Kovnats, Roger E. Stevenson and Charles E. Schwartz

    Article first published online : 21 JUN 1999, DOI: 10.1002/(SICI)1096-8628(19990730)85:3<255::AID-AJMG14>3.0.CO;2-Z

  12. Does unequal crossing over contribute to the mutation rate in Duchenne muscular dystrophy?

    American Journal of Medical Genetics

    Volume 12, Issue 4, August 1982, Pages: 437–441, Dr. R. M. Winter, M. E. Pembrey and John M. Opitz

    Article first published online : 2 JUN 2005, DOI: 10.1002/ajmg.1320120407

  13. Linkage analysis in Spanish families with nonspecific X-linked mental retardation: Significant linkage at Xq13–q21

    American Journal of Medical Genetics

    Volume 98, Issue 4, 1 February 2001, Pages: 343–347, Celia Badenas, Sergi Castellví-Bel, Victor Volpini, Dolores Jiménez, Aurora Sánchez, Xavier Estivill and Montserrat Milà

    Article first published online : 19 JAN 2001, DOI: 10.1002/1096-8628(20010201)98:4<343::AID-AJMG1107>3.0.CO;2-V

  14. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: Possible new syndrome

    American Journal of Medical Genetics

    Volume 66, Issue 2, 11 December 1996, Pages: 179–183, Eva Seemanová and Ivan Lesný

    Article first published online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19961211)66:2<179::AID-AJMG10>3.0.CO;2-Q

  15. Application of benefit-to-cost analysis to an X-linked recessive cardiac and humeroperoneal neuromuscular disease

    American Journal of Medical Genetics

    Volume 6, Issue 4, 1980, Pages: 315–329, M. L. Wright and L. J. Elsas II

    Article first published online : 3 JUN 2005, DOI: 10.1002/ajmg.1320060409

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    X-linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma

    British Journal of Haematology

    Volume 152, Issue 1, January 2011, Pages: 13–30, Nima Rezaei, Elham Mahmoudi, Asghar Aghamohammadi, Rupali Das and Kim E. Nichols

    Article first published online : 18 NOV 2010, DOI: 10.1111/j.1365-2141.2010.08442.x

  17. You have free access to this content
    Physical, Psychological and Ethical issues in Caring for Individuals with Genetic Skin Disease

    Journal of Nursing Scholarship

    Volume 45, Issue 1, March 2013, Pages: 89–95, Diane C. Seibert and Thomas N. Darling

    Article first published online : 31 JAN 2013, DOI: 10.1111/jnu.12004

  18. Novel splicing mutation in the NEMO (IKK-gamma) gene with severe immunodeficiency and heterogeneity of X-chromosome inactivation

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 1, 1 January 2006, Pages: 31–39, Karen Helene Ørstavik, Marianne Kristiansen, Gun Peggy Knudsen, Kari Storhaug, Åshild Vege, Kristin Eiklid, Tore G Abrahamsen, Asma Smahi and Jon Steen-Johnsen

    Article first published online : 6 DEC 2005, DOI: 10.1002/ajmg.a.31026

  19. X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus

    Clinical Genetics

    Volume 42, Issue 3, September 1992, Pages: 114–121, R. W. Hendrlks, M. E. M. Kraakman and R. K. B. Schuurman

    Article first published online : 28 JUN 2008, DOI: 10.1111/j.1399-0004.1992.tb03221.x

  20. Genes on the X chromosome are important in undiagnosed mental retardation

    American Journal of Medical Genetics

    Volume 92, Issue 1, 1 May 2000, Pages: 57–61, Michael Partington, David Mowat, Stewart Einfeld, Bruce Tonge and Gillian Turner

    Article first published online : 25 APR 2000, DOI: 10.1002/(SICI)1096-8628(20000501)92:1<57::AID-AJMG10>3.0.CO;2-0