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Simple Search
Hits 1 – 5 of 5
1
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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2
Metformin treatment in young children with fragile X syndrome.
Biag, Hazel Maridith B
;
Potter, Laura A
;
Wilkins, Victoria
...
In: Molecular genetics & genomic medicine, vol 7, iss 11 (2019)
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3
A Pilot Quantitative Evaluation of Early Life Language Development in Fragile X Syndrome
Debra L. Reisinger
;
Rebecca C. Shaffer
;
Ernest V. Pedapati
...
In: Brain Sciences ; Volume 9 ; Issue 2 (2019)
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4
DDX3X and specific initiation factors modulate FMR1 repeat‐associated non‐AUG‐initiated translation
Linsalata, Alexander E
;
He, Fang
;
Malik, Ahmed M
. - : Wiley Periodicals, Inc., 2019
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5
Trastornos del habla en el síndrome X frágil. Una revisión bibliográfica ; Speech disorders in fragile X syndrome. A bibliographical review
Campos Guzmán, Miriam
;
Marín Suelves, Diana
;
Fernández Andrés, Mª Inmaculada
. - : Universidad de Granada, 2019
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