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Hits 1 – 3 of 3
1
Family history of FXTAS is associated with age-related cognitive-linguistic decline among mothers with the FMR1 premutation.
Klusek, Jessica
;
Fairchild, Amanda
;
Moser, Carly
...
In: Journal of neurodevelopmental disorders, vol 14, iss 1 (2022)
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2
Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family
Lahbib, Saida
;
Trabelsi, Mediha
;
Dallali, Hamza
...
In: ISSN: 0301-4851 ; EISSN: 1573-4978 ; Molecular Biology Reports ; https://hal-riip.archives-ouvertes.fr/pasteur-03565723 ; Molecular Biology Reports, Springer Verlag, 2019, 46 (4), pp.4185 - 4193. ⟨10.1007/s11033-019-04869-6⟩ (2019)
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3
The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies.
Steinberg, J
;
Webber, C
In: Symplectic Elements at Oxford ; Europe PubMed Central ; PubMed (http://www.ncbi.nlm.nih.gov/pubmed/) ; Web of Science (Lite) (http://apps.webofknowledge.com/summary.do) ; Scopus (http://www.scopus.com/home.url) ; CrossRef (2013)
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