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There are 1328 results for: content related to: Geographical distribution of Slovenian BRCA1 /2 families according to family origin: implications for genetic screening

  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. 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

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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

  6. Parents’ attitudes toward genetic testing of children for health conditions: A systematic review

    Clinical Genetics

    Q. Lim, B.C. McGill, V.F. Quinn, K.M. Tucker, D. Mizrahi, A.F. Patenaude, M. Warby, R.J. Cohn and C.E. Wakefield

    Version of Record online : 30 MAR 2017, DOI: 10.1111/cge.12989

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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

  8. 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

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

    Clinical Genetics

    X. Liu, Z. Han and C. Yang

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

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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. 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

  13. 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

  14. 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

  15. (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

  16. 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

  17. Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome

    Clinical Genetics

    Volume 87, Issue 6, June 2015, Pages: 507–516, G. Ponti, E. Castellsagué, C. Ruini, A. Percesepe and A. Tomasi

    Version of Record online : 9 DEC 2014, DOI: 10.1111/cge.12529

  18. 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

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    Genetics of Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome

    Clinical Genetics

    Volume 91, Issue 2, February 2017, Pages: 233–246, L. Fontana, B. Gentilin, L. Fedele, C. Gervasini and M. Miozzo

    Version of Record online : 16 NOV 2016, DOI: 10.1111/cge.12883

  20. Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing

    Clinical Genetics

    Volume 89, Issue 6, June 2016, Pages: 659–668, C. Mouden, C. Dubourg, W. Carré, S. Rose, C. Quelin, L. Akloul, H. Hamdi-Rozé, G. Viot, H. Salhi, P. Darnault, S. Odent, V. Dupé and V. David

    Version of Record online : 16 FEB 2016, DOI: 10.1111/cge.12722