コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 (encoding LIS1) cause lissencephaly, a human neuronal migration disorder.
2 cy of LIS1 results in lissencephaly, a human neuronal migration disorder.
3 r using nonrodent model systems for studying neuronal migration disorders.
4 correlation between pediatric epilepsies and neuronal migration disorders.
5 haracterised forms of muscular dystrophy and neuronal migration disorders.
6 y linking DYX1C1 with many genes involved in neuronal migration disorders.
7 ging from mild cognitive impairment (MCI) to neuronal migration disorders.
8 ogressive cognitive decline in patients with neuronal migration disorders.
9 otential to reveal common cellular causes of neuronal migration disorders.
12 mutated in X-linked lissencephaly (X-LIS), a neuronal migration disorder associated with epilepsy and
13 lissencephaly and double cortex are genetic neuronal migration disorders associated with mental reta
14 ales but manifests in females as a localized neuronal migration disorder, called periventricular nodu
15 so known as subcortical band heterotopia), a neuronal migration disorder causing epilepsy and mental
17 Cobblestone brain malformation (COB) is a neuronal migration disorder characterized by protrusions
18 ht into how cortactin and DCX, a known human neuronal migration disorder gene, participate in this pr
19 Periventricular heterotopia (PH) is a human neuronal migration disorder in which many neurons destin
20 ding these proteins in humans cause distinct neuronal migration disorders, including periventricular
21 ous deletions of 17p13.3 result in the human neuronal migration disorders isolated lissencephaly sequ
22 a gene whose hemi-deletion causes the human neuronal migration disorder Miller-Dieker lissencephaly.
26 (SBH) and lissencephaly (LIS), two distinct neuronal migration disorders producing epilepsy and vari
29 patients with occipitotemporal syndrome had neuronal migration disorder, suggesting a developmental
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。