(Q50123029)

25 February 2018

title

Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis. (English)

1 reference

25 February 2018

M Raynaud

4

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Didier Lacombe

object named as

D Lacombe

Brigitte Gilbert-Dussardier

2

0 references

3

object named as

B Gilbert-Dussardier

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25 February 2018

author name string

K Poirier

1

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25 February 2018

V Desportes

5

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25 February 2018

A P M de Brouwer

6

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25 February 2018

C Moraine

7

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25 February 2018

J P Fryns

8

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25 February 2018

H H Ropers

9

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25 February 2018

C Beldjord

10

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25 February 2018

J Chelly

11

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25 February 2018

T Bienvenu

12

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25 February 2018

publication date

19 October 2005

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25 February 2018

published in

Neurogenetics

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25 February 2018

volume

7

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25 February 2018

issue

1

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25 February 2018

page(s)

39-46

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25 February 2018

X-linked myoclonic epilepsy with spasticity and intellectual disability: mutation in the homeobox gene ARX

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-005-0014-0

ARX mutations in X-linked lissencephaly with abnormal genitalia

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10048-005-0014-0

Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy

21 January 2018

1 reference

12 December 2020

Recurrence risks in mental retardation

1 reference

12 December 2020

Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans

1 reference

12 December 2020

Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation

1 reference

12 December 2020

Clinical and behavioral characteristics in FG syndrome

1 reference

12 December 2020

The phenotypic spectrum of ARX mutations

1 reference

12 December 2020

ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation

1 reference

12 December 2020

Monogenic X-linked mental retardation: is it as frequent as currently estimated? The paradox of the ARX (Aristaless X) mutations.

1 reference

12 December 2020

Three new families with X-linked mental retardation caused by the 428-451dup(24bp) mutation in ARX.

1 reference

12 December 2020

Brain cysts associated with mutation in the Aristaless related homeobox gene, ARX.

1 reference

12 December 2020

Screening of the ARX gene in 682 retarded males.

1 reference

12 December 2020

Re-evaluation of MRX36 family after discovery of an ARX gene mutation reveals mild neurological features of Partington syndrome

1 reference

12 December 2020

Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation

1 reference

12 December 2020

ARX mutation in a boy with transsphenoidal encephalocele and hypopituitarism.

1 reference

12 December 2020

Denaturing high-performance liquid chromatography using the WAVE DNA fragment analysis system

1 reference

12 December 2020

Expression of a novel aristaless related homeobox gene 'Arx' in the vertebrate telencephalon, diencephalon and floor plate

1 reference

12 December 2020

10.1007/S10048-005-0014-0

Identifiers

DOI

1 reference

25 February 2018

1 reference

25 February 2018