(Q40232805)

18 September 2017

title

X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11. (English)

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18 September 2017

9

Gillian Turner

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18 September 2017

Lars Riff Jensen

1

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18 September 2017

Steffen Lenzner

2

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18 September 2017

Bettina Moser

3

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18 September 2017

Kristine Freude

4

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18 September 2017

Andreas Tzschach

5

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18 September 2017

Chen Wei

6

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18 September 2017

Jean-Pierre Fryns

7

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18 September 2017

Jamel Chelly

8

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18 September 2017

Claude Moraine

10

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18 September 2017

Ben Hamel

11

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18 September 2017

Hans-Hilger Ropers

12

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18 September 2017

Andreas Walter Kuss

13

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18 September 2017

publication date

13 September 2006

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European Journal of Human Genetics

18 September 2017

published in

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18 September 2017

volume

15

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18 September 2017

issue

1

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18 September 2017

page(s)

68-75

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X-linked mental retardation

18 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Nonsyndromic X-linked mental retardation: where are the missing mutations?

21 January 2018

1 reference

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Linkage studies with the gene for an X-linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Four families (MRX43, MRX44, MRX45, MRX52) with nonspecific X-linked mental retardation: Clinical and psychometric data and results of linkage analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

X-linked mental retardation: evidence for a recent mutation in a five-generation family (MRX65) linked to the pericentromeric region

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Systematic analysis of X-inactivation in 19XLMR families: extremely skewed profiles in carriers in three families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Novel syndromic form of X-linked complicated spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Primer design for large scale sequencing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

A new DNA sequence assembly program

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Mutations in the FTSJ1 gene coding for a novel S-adenosylmethionine-binding protein cause nonsyndromic X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Mutations in the JARID1C gene, which is involved in transcriptional regulation and chromatin remodeling, cause X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Mutations in PHF8 are associated with X linked mental retardation and cleft lip/cleft palate

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Molecular and comparative genetics of mental retardation

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Hearing silence: non-neutral evolution at synonymous sites in mammals

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

Mutations in the ZNF41 gene are associated with cognitive deficits: identification of a new candidate for X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

The structure and evolution of centromeric transition regions within the human genome

21 January 2018

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https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

The prevalence of mental retardation: a critical review of recent literature.

21 January 2018

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7 January 2021

Localization of the gene for Wieacker-Wolff syndrome in the pericentromeric region of the X chromosome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

7 January 2021

X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

7 January 2021

Pericentromeric genes for non-specific X-linked mental retardation (MRX)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

7 January 2021

Further linkage evidence for localization of mutational sites for nonsyndromic types of X-linked mental retardation at the pericentromeric region

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201714

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201714

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Dimensions Publication ID

18 September 2017

1031012737

0 references

1 reference