Endocrine Dysfunction in Female FMR1 Premutation Carriers: Characteristics and Association with Ill Health

By Campbell Sonya   Eley Sarah E. A.   McKechanie Andrew G.   Stanfield Andrew C.  

Genes, Vol. 7, Iss. 11, 2016-11 ,pp. : 101-101

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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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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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Molecular Correlates and Recent Advancements in the Diagnosis and Screening of FMR1-Related Disorders

By Rajan-Babu Indhu-Shree   Chong Samuel S.  

Genes, Vol. 7, Iss. 10, 2016-10 ,pp. : 87-87

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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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