Cell migration and cerebral cortical development (Q34216765)

31 July 2017

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title

Cell migration and cerebral cortical development (English)

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31 July 2017

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Golden JA

1

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31 July 2017

language of work or name

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1 February 2001

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Neuropathology and Applied Neurobiology

31 July 2017

published in

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31 July 2017

volume

27

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31 July 2017

issue

1

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31 July 2017

page(s)

22-28

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A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

31 July 2017

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Diagnostic criteria for Walker-Warburg syndrome

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Lissencephaly and other malformations of cortical development: 1995 update

21 January 2018

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Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly

21 January 2018

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Lissencephaly associated with cerebellar hypoplasia and myoclonic epilepsy in a Bedouin kindred: a new syndrome?

21 January 2018

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Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.

21 January 2018

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Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

21 January 2018

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Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons

21 January 2018

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Lissencephaly-pachygyria associated with congenital cytomegalovirus infection.

21 January 2018

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Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

21 January 2018

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Norman-Roberts syndrome: clinical and molecular studies

21 January 2018

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An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

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Lissencephaly associated with congenital hypomyelinating and axonal neuropathy

21 January 2018

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Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients

21 January 2018

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LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

21 January 2018

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Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

21 January 2018

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Development of the cortical dysplasia of type II lissencephaly

21 January 2018

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Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration

21 January 2018

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Genetic malformations of the human cerebral cortex

21 January 2018

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Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

21 January 2018

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10.1046/J.0305-1846.2001.00307.X

21 January 2018

Identifiers

DOI

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31 July 2017

1 reference