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There are 40393 results for: content related to: Intrafamilial phenotypic variability in four families with Anderson-Fabry disease

  1. National mutation study among Danish patients with hereditary haemorrhagic telangiectasia

    Clinical Genetics

    Volume 86, Issue 2, August 2014, Pages: 123–133, P.M. Tørring, K. Brusgaard, L.B. Ousager, P.E. Andersen and A.D. Kjeldsen

    Version of Record online : 3 OCT 2013, DOI: 10.1111/cge.12269

  2. Changes in soil nutrient content and bacterial community after 12 years of organic amendment application to a vineyard

    European Journal of Soil Science

    Volume 66, Issue 4, July 2015, Pages: 802–812, M. E. Calleja-Cervantes, S. Menéndez, A. J. Fernández-González, I. Irigoyen, J. F. Cibriáin-Sabalza, N. Toro, P. M. Aparicio-Tejo and M. Fernández-López

    Version of Record online : 14 MAY 2015, DOI: 10.1111/ejss.12261

  3. You have free access to this content
    X-chromosome inactivation in female patients with Fabry disease

    Clinical Genetics

    Volume 89, Issue 1, January 2016, Pages: 44–54, L. Echevarria, K. Benistan, A. Toussaint, O. Dubourg, A.A. Hagege, D. Eladari, F. Jabbour, C. Beldjord, P. De Mazancourt and D.P. Germain

    Version of Record online : 22 JUN 2015, DOI: 10.1111/cge.12613

  4. An Investigation of Supervisory Practices to Develop Relational and Reflective Competence in Psychologists

    Australian Psychologist

    Volume 52, Issue 6, December 2017, Pages: 467–479, Fiona L. Calvert, Trevor P. Crowe and Brin F. S. Grenyer

    Version of Record online : 30 JAN 2017, DOI: 10.1111/ap.12261

  5. Geographical and ethnic distribution of MTHFR gene polymorphisms and their associations with diseases among Chinese population

    Clinical Genetics

    Volume 92, Issue 3, September 2017, Pages: 243–258, B. Yang, S. Fan, X. Zhi, R. Xia, Y. Wang, Q. Zheng and G. Sun

    Version of Record online : 15 MAR 2017, DOI: 10.1111/cge.12929

  6. Human leucocyte antigen alloimmunisation in repeatedly transfused thalassemic Egyptian children and its relation to febrile non-haemolytic transfusion reactions

    Transfusion Medicine

    Volume 25, Issue 6, December 2015, Pages: 380–384, Z. Mourad, H. Hassab, D. Younan and A. Abdo

    Version of Record online : 17 NOV 2015, DOI: 10.1111/tme.12261

  7. Modeling effects of SGLT-2 inhibitor dapagliflozin treatment versus standard diabetes therapy on cardiovascular and microvascular outcomes

    Diabetes, Obesity and Metabolism

    Volume 16, Issue 7, July 2014, Pages: 628–635, J. Dziuba, P. Alperin, J. Racketa, U. Iloeje, D. Goswami, E. Hardy, I. Perlstein, H. L. Grossman and M. Cohen

    Version of Record online : 19 FEB 2014, DOI: 10.1111/dom.12261

  8. Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation

    Clinical Genetics

    Volume 86, Issue 3, September 2014, Pages: 238–245, S. Sheikhzadeh, C. Sondermann, M. Rybczynski, C.R. Habermann, L. Brockstaedt, B. Keyser, H. Kaemmerer, T. Mir, A. Staebler, P.N. Robinson, K. Kutsche, J. Berger, S. Blankenberg and Y. von Kodolitsch

    Version of Record online : 23 SEP 2013, DOI: 10.1111/cge.12264

  9. Novel B3GALTL mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes

    Clinical Genetics

    Volume 86, Issue 2, August 2014, Pages: 142–148, E. Weh, L.M. Reis, R.C. Tyler, D. Bick, W.J. Rhead, S. Wallace, T.L. McGregor, S.K. Dills, M.-C. Chao, J.C. Murray and E.V. Semina

    Version of Record online : 17 SEP 2013, DOI: 10.1111/cge.12241

  10. Exploration of the cognitive, adaptive and behavioral functioning of patients affected with Bardet–Biedl syndrome

    Clinical Genetics

    Volume 89, Issue 4, April 2016, Pages: 426–433, E. N. Kerr, A. Bhan and E. Héon

    Version of Record online : 16 JUN 2015, DOI: 10.1111/cge.12614

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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

  12. You have free access to this content
    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

  13. The psychological impact of breast and ovarian cancer preventive options in BRCA1 and BRCA2 mutation carriers

    Clinical Genetics

    Volume 85, Issue 1, January 2014, Pages: 7–15, C Borreani, S Manoukian, E Bianchi, C Brunelli, B Peissel, A Caruso, G Morasso and MA Pierotti

    Version of Record online : 5 NOV 2013, DOI: 10.1111/cge.12298

  14. You have free access to this content
    Investigation of black and brown carbon multiple-wavelength-dependent light absorption from biomass and fossil fuel combustion source emissions

    Journal of Geophysical Research: Atmospheres

    Volume 120, Issue 13, 16 July 2015, Pages: 6682–6697, Michael R. Olson, Mercedes Victoria Garcia, Michael A. Robinson, Paul Van Rooy, Mark A. Dietenberger, Michael Bergin and James Jay Schauer

    Version of Record online : 14 JUL 2015, DOI: 10.1002/2014JD022970

  15. School Staff Perspectives on the Challenges and Solutions to Working With Court-Involved Students

    Journal of School Health

    Volume 85, Issue 6, June 2015, Pages: 347–354, Shantel D. Crosby, Angelique G. Day, Beverly A. Baroni and Cheryl L. Somers

    Version of Record online : 15 APR 2015, DOI: 10.1111/josh.12261

  16. Vascular risk factors in children, adolescents, and young adults with type 1 diabetes complicated by celiac disease: results from the DPV initiative

    Pediatric Diabetes

    Volume 17, Issue 3, May 2016, Pages: 191–198, Katharina Warncke, Susanne Liptay, Elke Fröhlich-Reiterer, Nicole Scheuing, Martin Schebek, Johannes Wolf, Tilman R. Rohrer, Thomas Meissner and Reinhard W. Holl

    Version of Record online : 12 FEB 2015, DOI: 10.1111/pedi.12261

  17. Phenotype–genotype correlations in patients with Marinesco–Sjögren syndrome

    Clinical Genetics

    Volume 86, Issue 1, July 2014, Pages: 74–84, F. Ezgu, P. Krejci, S. Li, C. de Sousa, J.M. Graham Jr, I. Hansmann, W. He, K. Porpora, D. Wand, W. Wertelecki, A. Schneider and W.R. Wilcox

    Version of Record online : 30 JUL 2013, DOI: 10.1111/cge.12230

  18. Two novel mutations in apolipoprotein C3 underlie atheroprotective lipid profiles in families

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 433–440, A.E. Bochem, J.C. van Capelleveen, G.M. Dallinga-Thie, A.W.M. Schimmel, M.M. Motazacker, I. Tietjen, R.R. Singaraja, M.R. Hayden, J.J.P. Kastelein, E.S.G. Stroes and G.K. Hovingh

    Version of Record online : 24 JUN 2013, DOI: 10.1111/cge.12201

  19. Deals not done: Sources of failure in the market for ideas

    Strategic Management Journal

    Volume 36, Issue 7, July 2015, Pages: 976–986, Ajay Agrawal, Iain Cockburn and Laurina Zhang

    Version of Record online : 18 APR 2014, DOI: 10.1002/smj.2261

  20. Recognizing the tenascin-X deficient type of Ehlers–Danlos syndrome: a cross-sectional study in 17 patients

    Clinical Genetics

    Volume 91, Issue 3, March 2017, Pages: 411–425, S. Demirdas, E. Dulfer, L. Robert, M. Kempers, D. van Beek, D. Micha, B.G. van Engelen, B. Hamel, J. Schalkwijk, B. Loeys, A. Maugeri and N.C. Voermans

    Version of Record online : 4 NOV 2016, DOI: 10.1111/cge.12853