Search Results

There are 3913 results for: content related to: From mouse to humans: discovery of the CACNG2 pain susceptibility gene

  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

  3. 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

  4. You have free access to this content
    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

  5. Epigenetic changes in diabetes

    Clinical Genetics

    Volume 84, Issue 1, July 2013, Pages: 1–10, ST Keating and A El-Osta

    Version of Record online : 11 MAR 2013, DOI: 10.1111/cge.12121

  6. Clinical and genetic heterogeneity of amyotrophic lateral sclerosis

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 408–416, M Sabatelli, A Conte and M Zollino

    Version of Record online : 12 MAR 2013, DOI: 10.1111/cge.12117

  7. You have free access to this content
    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

  8. You have free access to this content
    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

  9. 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

  10. Galactose-1-phosphate uridyltransferase deficiency: A literature review of the putative mechanisms of short and long-term complications and allelic variants

    Clinical Genetics

    E. Viggiano, A. Marabotti, L. Politano and A. Burlina

    Version of Record online : 9 AUG 2017, DOI: 10.1111/cge.13030

  11. Genetics of hypertrophic cardiomyopathy: A review of current state

    Clinical Genetics

    M. Sabater-Molina, I. Pérez-Sánchez, J.P. Hernández del Rincón and J.R. Gimeno

    Version of Record online : 17 AUG 2017, DOI: 10.1111/cge.13027

  12. You have free access to this content
    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

  13. 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

  14. The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 303–314, FC Connell, K Gordon, G Brice, V Keeley, S Jeffery, PS Mortimer, S Mansour and P Ostergaard

    Version of Record online : 27 JUN 2013, DOI: 10.1111/cge.12173

  15. Molecular cytogenetics: recent developments and applications in cancer

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 315–325, K Das and P Tan

    Version of Record online : 6 AUG 2013, DOI: 10.1111/cge.12229

  16. 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

  17. You have free access to this content
    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

  18. 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

  19. 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

  20. 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