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There are 21673 results for: content related to: Recommendations for the predictive genetic test in Huntington's disease

  1. You have free access to this content
    Single gene defects leading to sperm quantitative anomalies

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 208–216, M.J. Mitchell, C. Metzler-Guillemain, A. Toure, C. Coutton, C. Arnoult and P.F. Ray

    Version of Record online : 22 NOV 2016, DOI: 10.1111/cge.12900

  2. Evidence-based genetic counselling implications for Huntington disease intermediate allele predictive test results

    Clinical Genetics

    Volume 85, Issue 4, April 2014, Pages: 303–311, A. Semaka and M.R. Hayden

    Version of Record online : 15 JAN 2014, DOI: 10.1111/cge.12324

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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

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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

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    Drosophila as a tool for studying the conserved genetics of pain

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 359–366, G Milinkeviciute, C Gentile and G Gregory Neely

    Version of Record online : 22 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01941.x

  6. BMP15 “knockout-like” effect in familial premature ovarian insufficiency with persistent ovarian reserve

    Clinical Genetics

    Volume 92, Issue 2, August 2017, Pages: 208–212, A. Mayer, B. Fouquet, M. Pugeat and M. Misrahi

    Version of Record online : 30 MAR 2017, DOI: 10.1111/cge.12970

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    Twin studies of pain

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 331–340, CS Nielsen, GP Knudsen and ÓA Steingrímsdóttir

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01938.x

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    Nerve growth factor and the physiology of pain: lessons from congenital insensitivity to pain with anhidrosis

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 341–350, Y Indo

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01943.x

  9. The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing

    Clinical Genetics

    Volume 86, Issue 3, September 2014, Pages: 207–216, G.M. Christenhusz, K. Devriendt, H. Peeters, H. Van Esch and K. Dierickx

    Version of Record online : 6 MAR 2014, DOI: 10.1111/cge.12354

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    Genetic aspects of sodium channelopathy in small fiber neuropathy

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 351–358, JGJ Hoeijmakers, ISJ Merkies, MM Gerrits, SG Waxman and CG Faber

    Version of Record online : 7 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01937.x

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    From mouse to humans: discovery of the CACNG2 pain susceptibility gene

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 311–320, J Nissenbaum

    Version of Record online : 26 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01924.x

  12. Intrafamilial phenotypic variability in four families with Anderson-Fabry disease

    Clinical Genetics

    Volume 86, Issue 3, September 2014, Pages: 258–263, M. Rigoldi, D. Concolino, A. Morrone, F. Pieruzzi, R. Ravaglia, F. Furlan, F. Santus, P. Strisciuglio, G. Torti and R. Parini

    Version of Record online : 20 SEP 2013, DOI: 10.1111/cge.12261

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    Human Mendelian pain disorders: a key to discovery and validation of novel analgesics

    Clinical Genetics

    Volume 82, Issue 4, October 2012, Pages: 367–373, YP Goldberg, SN Pimstone, R Namdari, N Price, C Cohen, RP Sherrington and MR Hayden

    Version of Record online : 13 AUG 2012, DOI: 10.1111/j.1399-0004.2012.01942.x

  14. Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locus

    Clinical Genetics

    Volume 83, Issue 3, March 2013, Pages: 251–256, SK Holman, T Morgan, G Baujat, V Cormier-Daire, T-J Cho, M Lees, J Samanich, D Tapon, HD Hove, A Hing, R Hennekam and SP Robertson

    Version of Record online : 5 JUL 2012, DOI: 10.1111/j.1399-0004.2012.01905.x

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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

  16. Polydactyly: phenotypes, genetics and classification

    Clinical Genetics

    Volume 85, Issue 3, March 2014, Pages: 203–212, S. Malik

    Version of Record online : 18 OCT 2013, DOI: 10.1111/cge.12276

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    Maternal genetic polymorphisms and unexplained recurrent miscarriage: a systematic review and meta-analysis

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 265–284, X. Shi, X. Xie, Y. Jia and S. Li

    Version of Record online : 30 NOV 2016, DOI: 10.1111/cge.12910

  18. 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

  19. 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

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    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