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There are 16129 results for: content related to: Analysis of the VCX3A , VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis

  1. Segregation analysis in X-linked ichthyosis: paternal transmission of the affected X-chromosome

    British Journal of Dermatology

    Volume 158, Issue 4, April 2008, Pages: 818–820, J. Toral-Lopez, L.M. González-Huerta and S.A. Cuevas-Covarrubias

    Article first published online : 17 JAN 2008, DOI: 10.1111/j.1365-2133.2007.08405.x

  2. Atypical X-linked ichthyosis in a patient with a large deletion involving the steroid sulfatase (STS) gene

    International Journal of Dermatology

    Volume 48, Issue 2, February 2009, Pages: 142–144, Luz Gonzalez-Huerta, Jaime Mendiola-Jimenez, Maria Del Moral-Stevenel, Maria Rivera-Vega and Sergio Cuevas-Covarrubias

    Article first published online : 19 JAN 2009, DOI: 10.1111/j.1365-4632.2009.03996.x

  3. You have free access to this content
    Functional dependence on calcineurin by variants of the Saccharomyces cerevisiae vacuolar Ca2+/H+ exchanger Vcx1p

    Molecular Microbiology

    Volume 54, Issue 4, November 2004, Pages: 1104–1116, Jon K. Pittman, Ning-Hui Cheng, Toshiro Shigaki, Madhurababu Kunta and Kendal D. Hirschi

    Article first published online : 22 SEP 2004, DOI: 10.1111/j.1365-2958.2004.04332.x

  4. Xp22.3 microdeletion including VCX-A and VCX-B1 genes in an X-linked ichthyosis family: no difference in deletion size for patients with and without mental retardation

    Clinical Genetics

    Volume 67, Issue 4, April 2005, Pages: 367–368,

    Article first published online : 22 FEB 2005, DOI: 10.1111/j.1399-0004.2005.00417.x

  5. Carrier identification by FISH analysis in isolated cases of X-linked ichthyosis

    American Journal of Medical Genetics

    Volume 102, Issue 2, 1 August 2001, Pages: 146–148, M. Valdes-Flores, S.H. Kofman-Alfaro, A.L. Jimenez-Vaca and S.A. Cuevas-Covarrubias

    Article first published online : 14 JUN 2001, DOI: 10.1002/ajmg.1450

  6. You have free access to this content
    Steroid sulfatase deficiency and contiguous gene deletion syndrome amongst pregnant patients with low serum unconjugated estriols

    Prenatal Diagnosis

    Volume 29, Issue 10, October 2009, Pages: 966–974, Sylvie Langlois, Linlea Armstrong, Kim Gall, Gurdip Hulait, Janet Livingston, Tanya Nelson, Patricia Power, Denise Pugash, Dawn Siciliano, Michelle Steinraths and André Mattman

    Article first published online : 16 JUL 2009, DOI: 10.1002/pd.2326

  7. The Xp contiguous deletion syndrome and autism

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 6, June 2009, Pages: 1138–1148, Marwan Shinawi, Ankita Patel, Prisana Panichkul, Roxanne Zascavage, Sarika U. Peters and Fernando Scaglia

    Article first published online : 13 MAY 2009, DOI: 10.1002/ajmg.a.32833

  8. Mendelian Disorders of Cornification (MEDOC): The Ichthyoses

    Harper's Textbook of Pediatric Dermatology, Volume 1, 2, Third Edition

    Daniel Hohl, Mary Williams, Pages: 121.1–121.70, 2011

    Published Online : 24 MAY 2011, DOI: 10.1002/9781444345384.ch121

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    Cytochrome c maturation system on the negative side of bioenergetic membranes: CCB or System IV

    FEBS Journal

    Volume 278, Issue 22, November 2011, Pages: 4189–4197, Catherine de Vitry

    Article first published online : 20 OCT 2011, DOI: 10.1111/j.1742-4658.2011.08373.x

  10. Pharmacological treatment for depression during opioid agonist treatment for opioid dependence

    Intervention Review

    The Cochrane Library

    Pier Paolo Pani, Rosangela Vacca, Emanuela Trogu, Laura Amato and Marina Davoli

    Published Online : 8 SEP 2010, DOI: 10.1002/14651858.CD008373.pub2

  11. Recycled pulsars with black hole companions: the high-mass analogues of PSR B2303+46

    Monthly Notices of the Royal Astronomical Society

    Volume 354, Issue 4, November 2004, Pages: L49–L53, M. S. Sipior, S. Portegies Zwart and G. Nelemans

    Article first published online : 18 OCT 2004, DOI: 10.1111/j.1365-2966.2004.08373.x

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    Coupling of perturbations in the solar wind density to global Pi3 pulsations: A case study

    Journal of Geophysical Research: Space Physics (1978–2012)

    Volume 112, Issue A5, May 2007, D.-S. Han, H.-G. Yang, Z.-T. Chen, T. Araki, M. W. Dunlop, M. Nosé, T. Iyemori, Q. Li, Y.-F. Gao and K. Yumoto

    Article first published online : 24 MAY 2007, DOI: 10.1029/2006JA011675

  13. You have full text access to this OnlineOpen article
    Structural basis for Pan3 binding to Pan2 and its function in mRNA recruitment and deadenylation

    The EMBO Journal

    Volume 33, Issue 14, 17 July 2014, Pages: 1514–1526, Jana Wolf, Eugene Valkov, Mark D Allen, Birthe Meineke, Yuliya Gordiyenko, Stephen H McLaughlin, Tayla M Olsen, Carol V Robinson, Mark Bycroft, Murray Stewart and Lori A Passmore

    Article first published online : 29 MAY 2014, DOI: 10.15252/embj.201488373

  14. Common structural features characterize interstitial intrachromosomal Xp and 18q triplications

    American Journal of Medical Genetics Part A

    Volume 155, Issue 11, November 2011, Pages: 2681–2687, Roberto Giorda, Silvana Beri, M. Clara Bonaglia, Luigina Spaccini, Barbara Scelsa, Emmanouil Manolakos, Erika Della Mina, Roberto Ciccone and Orsetta Zuffardi

    Article first published online : 30 SEP 2011, DOI: 10.1002/ajmg.a.34248

  15. Regulation of mRNA decapping

    Wiley Interdisciplinary Reviews: RNA

    Volume 1, Issue 2, September/October 2010, Pages: 253–265, You Li and Megerditch Kiledjian

    Article first published online : 6 MAY 2010, DOI: 10.1002/wrna.15

  16. Clinical utility of the X-chromosome array

    American Journal of Medical Genetics Part A

    Volume 161, Issue 1, January 2013, Pages: 120–130, Yuri A. Zarate, Alka Dwivedi, Frank O. Bartel, M. Allison Bellomo, Sara S. Cathey, Neena L. Champaigne, L. Kate Clarkson, Barbara R. DuPont, David B. Everman, Joseph S. Geer, Barbara C. Gordon, Angie W. Lichty, Michael J. Lyons, R. Curtis Rogers, Robert A. Saul, Richard J. Schroer, Steven A. Skinner and Roger E. Stevenson

    Article first published online : 3 DEC 2012, DOI: 10.1002/ajmg.a.35698

  17. Association of the steroid sulfatase (STS) gene with attention deficit hyperactivity disorder

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 147B, Issue 8, 5 December 2008, Pages: 1531–1535, K.J. Brookes, Z. Hawi, A. Kirley, E. Barry, M. Gill and L. Kent

    Article first published online : 20 OCT 2008, DOI: 10.1002/ajmg.b.30873

  18. Novel missense mutation (Arg432Cys) in a patient with steroid sulphatase-deficiency

    Clinical Endocrinology

    Volume 59, Issue 2, August 2003, Pages: 263–264, L. M. González-Huerta, M. R. Riviera-Vega, S. H. Kofman-Alfeuro and S. A. Cuevas-Covarrubias

    Article first published online : 16 JUL 2003, DOI: 10.1046/j.1365-2265.2003.17851.x

  19. Molecular cytogenetic analysis of a familial interstitial deletion Xp22.2-22.3 with a highly variable phenotype in female carriers

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 6, 15 March 2006, Pages: 604–610, Sylwia Chocholska, Eva Rossier, Gotthold Barbi and Hildegard Kehrer-Sawatzki

    Article first published online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31145

  20. The Late Jurassic Tithonian, a greenhouse phase in the Middle Jurassic–Early Cretaceous ‘cool’ mode: evidence from the cyclic Adriatic Platform, Croatia


    Volume 54, Issue 2, April 2007, Pages: 317–337, ANTUN HUSINEC and J. FRED READ

    Article first published online : 27 NOV 2006, DOI: 10.1111/j.1365-3091.2006.00837.x