(Q38901909)

7 September 2017

title

A locus for bilateral occipital polymicrogyria maps to chromosome 6q16-q22. (English)

1 reference

7 September 2017

0 references

Bouchra Ouled Amar Ben Cheikh

1

1 reference

7 September 2017

Stéphanie Baulac

2

1 reference

7 September 2017

Fatiha Lahjouji

3

1 reference

7 September 2017

Ahmed Bouhouche

4

1 reference

7 September 2017

Philippe Couarch

5

1 reference

7 September 2017

Naima Khalili

6

1 reference

7 September 2017

Wafae Regragui

7

1 reference

7 September 2017

Stéphane Lehericy

8

1 reference

7 September 2017

Merle Ruberg

9

1 reference

7 September 2017

Ali Benomar

10

1 reference

7 September 2017

Simon Heath

11

1 reference

7 September 2017

Taib Chkili

12

1 reference

7 September 2017

Mohamed Yahyaoui

13

1 reference

7 September 2017

Mohamed Jiddane

14

1 reference

7 September 2017

Reda Ouazzani

15

1 reference

7 September 2017

Eric LeGuern

16

1 reference

7 September 2017

publication date

29 August 2008

1 reference

7 September 2017

1 reference

7 September 2017

volume

10

1 reference

7 September 2017

issue

1

1 reference

7 September 2017

page(s)

35-42

1 reference

A developmental and genetic classification for malformations of cortical development

7 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Radiologic classification of malformations of cortical development

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

A familial syndrome of unilateral polymicrogyria affecting the right hemisphere.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Genetics of the polymicrogyria syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Congenital bilateral perisylvian syndrome: study of 31 patients. The CBPS Multicenter Collaborative Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

A locus for bilateral perisylvian polymicrogyria maps to Xq28

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

SRPX2 mutations in disorders of language cortex and cognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Genotype-phenotype analysis of human frontoparietal polymicrogyria syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

G protein-coupled receptor-dependent development of human frontal cortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Occipital lobe developmental malformations and epilepsy: clinical spectrum, treatment, and outcome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Occipital epilepsies: identification of specific and newly recognized syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Isolation of three novel human genes encoding G protein-coupled receptors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Pharmacological characterization of mouse GPRC6A, an L-alpha-amino-acid receptor modulated by divalent cations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

The rat GPRC6A: cloning and characterization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Neurotransmitters and brain maturation: early paracrine actions of GABA and glutamate modulate neuronal migration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

MICALs, a family of conserved flavoprotein oxidoreductases, function in plexin-mediated axonal repulsion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Defective limbic system in mice lacking the tailless gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Mutation and evolutionary analyses identify NR2E1-candidate-regulatory mutations in humans with severe cortical malformations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

MARCKS deficiency in mice leads to abnormal brain development and perinatal death

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10048-008-0143-3

Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment

21 January 2018

1 reference

12 December 2020

A new autosomal recessive syndrome of pachygyria.

1 reference

12 December 2020

Bilateral fronto-occipital polymicrogyria and epilepsy.

1 reference

12 December 2020

Familial Schizencephaly

1 reference

12 December 2020

Syndromes of bilateral symmetrical polymicrogyria

1 reference

12 December 2020

10.1007/S10048-008-0143-3

Identifiers

DOI

1 reference

release_5eh2tlqdx5d7tkfadryxfrhybi

7 September 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/5eh2tlqdx5d7tkfadryxfrhybi

24 November 2022

mapped directly with Wikidata item

1 reference