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Homozygous silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesisOligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardationX-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin familyTranscription factor SOX3 is involved in X-linked mental retardation with growth hormone deficiencyRecurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationMutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palateScreening of the 1 Mb SOX9 5' control region by array CGH identifies a large deletion in a case of campomelic dysplasia with XY sex reversalMutation screening of ASMT, the last enzyme of the melatonin pathway, in a large sample of patients with intellectual disabilityPre- and postnatal exposure to low dose glufosinate ammonium induces autism-like phenotypes in mice.The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients
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P50
description
hulumtues
@sq
onderzoeker
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researcher
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հետազոտող
@hy
name
Sylvain Briault
@ast
Sylvain Briault
@en
Sylvain Briault
@es
Sylvain Briault
@nl
Sylvain Briault
@sl
type
label
Sylvain Briault
@ast
Sylvain Briault
@en
Sylvain Briault
@es
Sylvain Briault
@nl
Sylvain Briault
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prefLabel
Sylvain Briault
@ast
Sylvain Briault
@en
Sylvain Briault
@es
Sylvain Briault
@nl
Sylvain Briault
@sl