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There are 4578 results for: content related to: Prevalence of restless legs syndrome and sleep quality in carriers of the fragile X premutation

  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. Fragile X syndrome: An overview and update of the FMR1 gene

    Clinical Genetics

    M. Mila, M.I. Alvarez-Mora, I. Madrigal and L. Rodriguez-Revenga

    Version of Record online : 1 OCT 2017, DOI: 10.1111/cge.13075

  3. Sociodemographic, psychosocial and clinical factors associated with uptake of genetic counselling for hereditary cancer: a systematic review

    Clinical Genetics

    Volume 92, Issue 2, August 2017, Pages: 121–133, A.M. Willis, S.K. Smith, B. Meiser, M.L. Ballinger, D.M. Thomas and M.-A. Young

    Version of Record online : 23 OCT 2016, DOI: 10.1111/cge.12868

  4. Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion

    Clinical Genetics

    Volume 87, Issue 2, February 2015, Pages: 173–178, D. Z. Loesch, M. Q. Bui, E. Hammersley, A. Schneider, E. Storey, P. Stimpson, T. Burgess, D. Francis, H. Slater, F. Tassone, R. J. Hagerman and D. Hessl

    Version of Record online : 17 FEB 2014, DOI: 10.1111/cge.12347

  5. A family with two female siblings with compound heterozygous FMR1 premutation alleles

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 458–463, K. Basuta, R. Lozano, A. Schneider, C.M. Yrigollen, D. Hessl, R.J. Hagerman and F. Tassone

    Version of Record online : 28 JUL 2013, DOI: 10.1111/cge.12218

  6. Frequency of FMR1 premutation carriers and rate of expansion to full mutation in a retrospective diagnostic FMR1 Korean sample

    Clinical Genetics

    Volume 85, Issue 5, May 2014, Pages: 441–445, J.-H. Jang, K. Lee, E.-H. Cho, E.-H. Lee, J.-W. Kim and C.-S. Ki

    Version of Record online : 13 JUN 2013, DOI: 10.1111/cge.12195

  7. Neurological and endocrine phenotypes of fragile X carrier women

    Clinical Genetics

    Volume 89, Issue 1, January 2016, Pages: 60–67, D. Hall, K. Todorova-Koteva, S. Pandya, B. Bernard, B. Ouyang, M. Walsh, T. Pounardjian, C. Deburghraeve, L. Zhou, M. Losh, M. Leehey and E. Berry-Kravis

    Version of Record online : 4 SEP 2015, DOI: 10.1111/cge.12646

  8. You have free access to this content
    Social anxiety and autism spectrum traits among adult FMR1 premutation carriers

    Clinical Genetics

    Volume 91, Issue 1, January 2017, Pages: 111–114, O. López-Mourelo, E. Mur, I. Madrigal, M.I. Alvarez-Mora, B. Gómez-Ansón, J. Pagonabarraga, L. Rodriguez-Revenga and M. Milà

    Version of Record online : 26 MAY 2016, DOI: 10.1111/cge.12791

  9. Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype–phenotype study

    Clinical Genetics

    Volume 92, Issue 5, November 2017, Pages: 477–486, C. Tardieu, S. Jung, K. Niederreither, M. Prasad, S. Hadj-Rabia, N. Philip, A. Mallet, E. Consolino, E. Sfeir, B. Noueiri, N. Chassaing, H. Dollfus, M.C. Manière, A. Bloch-Zupan and F. Clauss

    Version of Record online : 19 MAR 2017, DOI: 10.1111/cge.12972

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    Myotonic dystrophy type 1: role of CCG, CTC and CGG interruptions within DMPK alleles in the pathogenesis and molecular diagnosis

    Clinical Genetics

    Volume 92, Issue 4, October 2017, Pages: 355–364, M. Santoro, M. Masciullo, G. Silvestri, G. Novelli and A. Botta

    Version of Record online : 22 FEB 2017, DOI: 10.1111/cge.12954

  11. (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

  12. 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

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    Cornelia de Lange syndrome

    Clinical Genetics

    Volume 88, Issue 1, July 2015, Pages: 1–12, M.I. Boyle, C. Jespersgaard, K. Brøndum-Nielsen, A.-M. Bisgaard and Z. Tümer

    Version of Record online : 28 OCT 2014, DOI: 10.1111/cge.12499

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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

  15. Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases

    Clinical Genetics

    Volume 89, Issue 3, March 2016, Pages: 285–294, K. Rai, R. Pilarski, C.M. Cebulla and M.H. Abdel-Rahman

    Version of Record online : 14 JUL 2015, DOI: 10.1111/cge.12630

  16. Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes

    Clinical Genetics

    Volume 87, Issue 1, January 2015, Pages: 11–20, J.R. Cook, L. Carta, J. Galatioto and F. Ramirez

    Version of Record online : 10 JUL 2014, DOI: 10.1111/cge.12436

  17. Cross-border reprogenetic services

    Clinical Genetics

    Volume 87, Issue 1, January 2015, Pages: 1–10, V. Couture, R. Drouin, S.-L. Tan, J.-M. Moutquin and C. Bouffard

    Version of Record online : 6 JUN 2014, DOI: 10.1111/cge.12418

  18. The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features

    Clinical Genetics

    Volume 87, Issue 5, May 2015, Pages: 401–410, M. Ruggieri, A. Polizzi, A. Spalice, V. Salpietro, R. Caltabiano, V. D'Orazi, P. Pavone, C. Pirrone, G. Magro, N. Platania, S. Cavallaro, M. Muglia and F. Nicita

    Version of Record online : 22 NOV 2014, DOI: 10.1111/cge.12498

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    Panel-based testing for inherited colorectal cancer: a descriptive study of clinical testing performed by a US laboratory

    Clinical Genetics

    Volume 86, Issue 6, December 2014, Pages: 510–520, D. Cragun, C. Radford, J.S. Dolinsky, M. Caldwell, E. Chao and T. Pal

    Version of Record online : 20 MAR 2014, DOI: 10.1111/cge.12359

  20. FXTAS in an unmethylated mosaic male with fragile X syndrome from Chile

    Clinical Genetics

    Volume 86, Issue 4, October 2014, Pages: 378–382, L. Santa María, A. Pugin, M.A. Alliende, S. Aliaga, B. Curotto, T. Aravena, H.-T. Tang, G. Mendoza-Morales, R. Hagerman and F. Tassone

    Version of Record online : 13 OCT 2013, DOI: 10.1111/cge.12278