A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.
about
Neuronal Migration and AUTS2 Syndrome.NKL homeobox gene MSX1 acts like a tumor suppressor in NK-cell leukemia.Glycosphingolipid metabolic reprogramming drives neural differentiation.A low-grade astrocytoma in a sixteen-year-old boy with a 7q11.22 deletion.Mitochondrial dysfunction and autism: comprehensive genetic analyses of children with autism and mtDNA deletion.A novel truncating variant within exon 7 of KAT6B associated with features of both Say-Barber-Bieseker-Young-Simpson syndrome and genitopatellar syndrome: Further evidence of a continuum in the clinical spectrum of KAT6B-related disorders.Activity of Genes with Functions in Human Williams-Beuren Syndrome Is Impacted by Mobile Element Insertions in the Gray Wolf Genome.The Epigenetic Factor Landscape of Developing Neocortex Is Regulated by Transcription Factors Pax6→ Tbr2→ Tbr1
P2860
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P2860
A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
@zh-hans
2016年学术文章
@zh-my
2016年学术文章
@zh-sg
2016年學術文章
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2016年學術文章
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2016年學術文章
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name
A detailed clinical analysis o ...... res the behavioural phenotype.
@en
A detailed clinical analysis o ...... res the behavioural phenotype.
@nl
type
label
A detailed clinical analysis o ...... res the behavioural phenotype.
@en
A detailed clinical analysis o ...... res the behavioural phenotype.
@nl
prefLabel
A detailed clinical analysis o ...... res the behavioural phenotype.
@en
A detailed clinical analysis o ...... res the behavioural phenotype.
@nl
P2093
P2860
P1476
A detailed clinical analysis o ...... res the behavioural phenotype.
@en
P2093
Alex C Magee
Bart Elffers
Berten Ceulemans
Elizabeth J Meijers-Heijboer
Erik A Sistermans
Gea Beunders
Helger G Yntema
Janneke Schuurs-Hoeijmakers
Jenny Morton
P2860
P304
P356
10.1136/JMEDGENET-2015-103601
P407
P50
P577
2016-04-13T00:00:00Z