Publications by authors named "Sylviane Marouillat"

14Publications

Mutation screening of the ubiquitin ligase gene RNF135 in French patients with autism.

Psychiatr Genet 2015 Dec;25(6):263-7

aUMR INSERM U930, University François-Rabelais bCHRU Tours, Department of Pedopsychiatry cCHRU Tours, Department of Biochemistry and Molecular Biology dCNRS UPR 4301, CBM, Orléans.

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http://dx.doi.org/10.1097/YPG.0000000000000100DOI Listing
December 2015

Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems.

Am J Hum Genet 2015 Mar 19;96(3):386-96. Epub 2015 Feb 19.

Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud university medical center, Nijmegen 6500 HB, the Netherlands; Department of Cognitive Neurosciences, Donders Institute for Brain, Cognition, and Behavior, Radboud university medical center, Nijmegen 6500 HB, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2015.01.010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4375531PMC
March 2015

Mutation screening and association study of the UBE2H gene on chromosome 7q32 in autistic disorder.

Psychiatr Genet 2003 Dec;13(4):221-5

Génétique de la déficience mentale et de l'autisme, INSERM U316, Faculté de Médecine, Tours, France.

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http://dx.doi.org/10.1097/00041444-200312000-00005DOI Listing
December 2003

Molecular analysis of the oligodendrocyte myelin glycoprotein gene in autistic disorder.

Neurosci Lett 2003 Feb;338(2):115-8

Génétique de la Déficience Mentale et de l'Autisme, INSERM U 316, Faculté de Médecine, 2bis, Boulevard Tonnellé, 37032, Tours Cedex, France.

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http://dx.doi.org/10.1016/s0304-3940(02)01338-1DOI Listing
February 2003