المؤلفون: Hocking, DR, Birch, RC, Bui, QM, Menant, JC, Lord, SR, Georgiou-Karistianis, N, Godler, DE, Wen, W, Hackett, A, Rogers, C, Trollor, JN

المصدر: urn:ISSN:0197-4580 ; urn:ISSN:1558-1497 ; Neurobiology of Aging, 50, 5-12

مصطلحات موضوعية: Fragile X Syndrome, Rare Diseases, Neurosciences, Behavioral and Social Science, Intellectual and Developmental Disabilities (IDD), Genetics, Brain Disorders, Clinical Research, Adult, Aged, Cerebellum, Cognition, Fragile X Mental Retardation Protein, Heterozygote, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Mutation, Neuroimaging, Postural Balance, RNA, Messenger, Reaction Time, Trinucleotide Repeats, Cerebellar motor networks, Choice stepping reaction time, Cognitive-motor interference, FMR1 premutation carrier, Fragile X mental retardation gene 1 (FMR1)

وصف الملف: application/pdf

العلاقة: http://purl.org/au-research/grants/arc/DP110103346Test; http://hdl.handle.net/1959.4/unsworks_41941Test; https://unsworks.unsw.edu.au/bitstreams/4338dc16-2b0b-4fb5-ac73-e1bd357cd57e/downloadTest; https://doi.org/10.1016/j.neurobiolaging.2016.10.017Test

الإتاحة: https://doi.org/10.1016/j.neurobiolaging.2016.10.017Test
http://hdl.handle.net/1959.4/unsworks_41941Test
https://unsworks.unsw.edu.au/bitstreams/4338dc16-2b0b-4fb5-ac73-e1bd357cd57e/downloadTest

المؤلفون: Hocking, Darren R., Birch, Rachael C., Trollor, Julian N., Bui, Quang M., Menant, Jasmine C., Lord, Stephen R., Georgiou-Karistianis, Nellie, Godler, David E., Wen, Wei, Hackett, Anna, Rogers, Carolyn

المساهمون: The University of Newcastle. Faculty of Health & Medicine, School of Biomedical Sciences and Pharmacy

مصطلحات موضوعية: FMR1 premutation carrier, fragile X mental retardation gene 1 (FMR1), cerebellar motor networks, cognitive-motor interference, step initiation, choice stepping reaction time, motor symptoms, postural balance

العلاقة: Neurobiology of Aging Vol. 50, Issue February 2017, p. 5-12; http://hdl.handle.net/1959.13/1384405Test; uon:32065

الإتاحة: http://hdl.handle.net/1959.13/1384405Test

المؤلفون: Voorhuis, M., Onland-Moret, N. C., Janse, F., van Amstel, H. K. Ploos, Goverde, A. J., Lambalk, C. B., Laven, J. S. E., van der Schouw, Y. T., Broekmans, F. J. M., Fauser, B. C. J. M., Hoek, Annemieke

المصدر: Voorhuis , M , Onland-Moret , N C , Janse , F , van Amstel , H K P , Goverde , A J , Lambalk , C B , Laven , J S E , van der Schouw , Y T , Broekmans , F J M , Fauser , B C J M , Dutch Primary Ovarian Insufficienc & Hoek , A 2014 , ' The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency ' , Human Reproduction , vol. 29 , ....

مصطلحات موضوعية: fragile X mental retardation gene 1, CGG repeats, menopause, primary ovarian insufficiency, ovarian ageing, FMR1 GENE, PREMUTATION CARRIERS, NATURAL MENOPAUSE, INFERTILE WOMEN, FAILURE, ASSOCIATION, POPULATION, NUMBER, AGE, IDENTIFICATION

العلاقة: https://research.rug.nl/en/publications/9fc4c823-c130-45ee-8114-c46f7b4695bcTest

الإتاحة: https://doi.org/10.1093/humrep/deu095Test
https://hdl.handle.net/11370/9fc4c823-c130-45ee-8114-c46f7b4695bcTest
https://research.rug.nl/en/publications/9fc4c823-c130-45ee-8114-c46f7b4695bcTest