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There are 5960 results for: content related to: Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucoma

  1. You have free access to this content
    Genetics of primary ovarian insufficiency

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 183–198, R. Rossetti, I. Ferrari, M. Bonomi and L. Persani

    Version of Record online : 12 DEC 2016, DOI: 10.1111/cge.12921

  2. Genetics of human Bardet–Biedl syndrome, an updates

    Clinical Genetics

    Volume 90, Issue 1, July 2016, Pages: 3–15, S.A. Khan, N. Muhammad, M.A. Khan, A. Kamal, Z.U. Rehman and S. Khan

    Version of Record online : 9 FEB 2016, DOI: 10.1111/cge.12737

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    Genetic abnormalities leading to qualitative defects of sperm morphology or function

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 217–232, P.F. Ray, A. Toure, C. Metzler-Guillemain, M.J. Mitchell, C. Arnoult and C. Coutton

    Version of Record online : 9 DEC 2016, DOI: 10.1111/cge.12905

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    The biology of germ cell tumors in disorders of sex development

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 292–301, Remko Hersmus, Yolande van Bever, Katja P. Wolffenbuttel, Katharina Biermann, Martine Cools and Leendert H.J. Looijenga

    Version of Record online : 24 NOV 2016, DOI: 10.1111/cge.12882

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    Recent insights on the genetics and epigenetics of endometriosis

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 254–264, B. Borghese, K.T. Zondervan, M.S. Abrao, C. Chapron and D. Vaiman

    Version of Record online : 30 NOV 2016, DOI: 10.1111/cge.12897

  6. Prenatal diagnosis of congenital myopathies and muscular dystrophies

    Clinical Genetics

    Volume 90, Issue 3, September 2016, Pages: 199–210, D. Massalska, J.G. Zimowski, J. Bijok, A. Kucińska-Chahwan, A. Łusakowska, G. Jakiel and T. Roszkowski

    Version of Record online : 2 JUN 2016, DOI: 10.1111/cge.12801

  7. Cardiovascular pharmacogenetics: a promise for genomically-guided therapy and personalized medicine

    Clinical Genetics

    Volume 91, Issue 3, March 2017, Pages: 355–370, M. Zaiou and H. El Amri

    Version of Record online : 30 NOV 2016, DOI: 10.1111/cge.12881

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    Genetics of the corneal endothelial dystrophies: an evidence-based review

    Clinical Genetics

    Volume 84, Issue 2, August 2013, Pages: 109–119, A J Aldave, J Han and R F Frausto

    Version of Record online : 10 JUN 2013, DOI: 10.1111/cge.12191

  9. Associations of microRNA single nucleotide polymorphisms and disease risk and pathophysiology

    Clinical Genetics

    Volume 92, Issue 3, September 2017, Pages: 235–242, X. Liu, Z. Han and C. Yang

    Version of Record online : 19 MAR 2017, DOI: 10.1111/cge.12950

  10. Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes

    Clinical Genetics

    C. Lintas and A.M. Persico

    Version of Record online : 1 MAR 2017, DOI: 10.1111/cge.12983

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    The genetic make-up of ovarian development and function: the focus on the transcription factor FOXL2

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 173–182, M. Elzaiat, A.-L. Todeschini, S. Caburet and R.A. Veitia

    Version of Record online : 29 SEP 2016, DOI: 10.1111/cge.12862

  12. Genetic and epigenetic insights into uveal melanoma

    Clinical Genetics

    A. Sharma, M.M. Stei, H. Fröhlich, F.G. Holz, K.U. Loeffler and M.C. Herwig-Carl

    Version of Record online : 24 JAN 2018, DOI: 10.1111/cge.13136

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    Pharmacogenetics of pain and analgesia

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 321–330, MT Smith and A Muralidharan

    Version of Record online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01936.x

  14. Spinocerebellar ataxia: relationship between phenotype and genotype – a review

    Clinical Genetics

    Volume 90, Issue 4, October 2016, Pages: 305–314, Y.-M. Sun, C. Lu and Z.-Y. Wu

    Version of Record online : 30 JUN 2016, DOI: 10.1111/cge.12808

  15. Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2

    Clinical Genetics

    Volume 91, Issue 5, May 2017, Pages: 661–671, G.C. Dworschak, C. Crétolle, A. Hilger, H. Engels, E. Korsch, H. Reutter and M. Ludwig

    Version of Record online : 10 OCT 2016, DOI: 10.1111/cge.12848

  16. Hearing loss in Waardenburg syndrome: a systematic review

    Clinical Genetics

    Volume 89, Issue 4, April 2016, Pages: 416–425, J. Song, Y. Feng, F.R. Acke, P. Coucke, K. Vleminckx and I.J. Dhooge

    Version of Record online : 17 JUL 2015, DOI: 10.1111/cge.12631

  17. Protein misfolding diseases: Prospects of pharmacological treatment

    Clinical Genetics

    A. Gámez, P. Yuste-Checa, S. Brasil, Á. Briso-Montiano, L.R. Desviat, M. Ugarte, C. Pérez-Cerdá and B. Pérez

    Version of Record online : 4 DEC 2017, DOI: 10.1111/cge.13088

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    Opioid genetics: the key to personalized pain control?

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 301–310, R Branford, J Droney and JR Ross

    Version of Record online : 26 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01923.x

  19. (Epi)genotype–phenotype correlations in Beckwith–Wiedemann syndrome: a paradigm for genomic medicine

    Clinical Genetics

    Volume 89, Issue 4, April 2016, Pages: 403–415, A. Mussa, S. Russo, L. Larizza, A. Riccio and G.B. Ferrero

    Version of Record online : 30 JUL 2015, DOI: 10.1111/cge.12635

  20. Clinical implementation of NIPT – technical and biological challenges

    Clinical Genetics

    Volume 89, Issue 5, May 2016, Pages: 523–530, P. Brady, N. Brison, K. Van Den Bogaert, T. de Ravel, H. Peeters, H. Van Esch, K. Devriendt, E. Legius and J.R. Vermeesch

    Version of Record online : 4 MAY 2015, DOI: 10.1111/cge.12598