Towards a Better Molecular Diagnosis of FMR1-Related Disorders—A Multiyear Experience from a Reference Lab

By Rzońca Sylwia Olimpia   Gos Monika   Szopa Daniel   Sielska-Rotblum Danuta   Landowska Aleksandra   Szpecht-Potocka Agnieszka   Milewski Michał   Czekajska Jolanta   Abramowicz Anna   Obersztyn Ewa   Maciejko Dorota   Mazurczak Tadeusz   Bal Jerzy  

Genes, Vol. 7, Iss. 9, 2016-09 ,pp. : 59-59

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Development of Genetic Testing for Fragile X Syndrome and Associated Disorders, and Estimates of the Prevalence of FMR1 Expansion Mutations

By Macpherson James N.   Murray Anna  

Genes, Vol. 7, Iss. 12, 2016-11 ,pp. : 110-110

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Associated Clinical Disorders Diagnosed by Medical Specialists in 188 FMR1 Premutation Carriers Found in the Last 25 Years in the Spanish Basque Country: A Retrospective Study

By Merino Sonia   Ibarluzea Nekane   Maortua Hiart   Prieto Begoña   Rouco Idoia   López-Aríztegui Maria-Asunción   Tejada Maria-Isabel  

Genes, Vol. 7, Iss. 10, 2016-10 ,pp. : 90-90

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Shaping the Cell and the Future: Recent Advancements in Biophysical Aspects Relevant to Regenerative Medicine

By Hart Melanie L.   Lauer Jasmin C.   Selig Mischa   Hanak Martha   Walters Brandan   Rolauffs Bernd  

Journal of Functional Morphology and Kinesiology, Vol. 3, Iss. 1, 2017-12 ,pp. : 2-2

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Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 Gene

By Barasoain Maitane   Barrenetxea Gorka   Huerta Iratxe   Télez Mercedes   Criado Begoña   Arrieta Isabel  

Genes, Vol. 7, Iss. 12, 2016-12 ,pp. : 123-123

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