(Q41919440)

14 October 2017

title

TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions (English)

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14 October 2017

12

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14 October 2017

Liesbeth Rooms

1

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14 October 2017

Edwin Reyniers

2

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14 October 2017

Stefaan Scheers

3

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14 October 2017

Rob van Luijk

4

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14 October 2017

Jan Wauters

5

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14 October 2017

Leen Van Aerschot

6

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14 October 2017

Zsuzsanna Callaerts-Vegh

7

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14 October 2017

Rudi D'Hooge

8

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14 October 2017

Gabrielle Mengus

9

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14 October 2017

Irwin Davidson

10

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14 October 2017

Winnie Courtens

11

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14 October 2017

publication date

14 June 2006

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European Journal of Human Genetics

14 October 2017

published in

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14 October 2017

volume

14

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14 October 2017

issue

10

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14 October 2017

page(s)

1090-1096

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201674

14 October 2017

exact match

0 references

cites work

Telomeres: a diagnosis at the end of the chromosomes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Subtelomeric rearrangements in the mentally retarded: a comparison of detection methods.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Subtelomeric deletions of chromosome 9q: a novel microdeletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Disruption of the gene Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) is associated with the 9q34 subtelomeric deletion syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Calibration of 6q subtelomere deletions to define genotype/phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

6q subtelomeric deletion: is there a recognizable syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Multiplex ligation-dependent probe amplification to detect subtelomeric rearrangements in routine diagnostics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Neurocognitive and psychotiform behavioral alterations and enhanced hippocampal long-term potentiation in transgenic mice displaying neuropathological features of human alpha-mannosidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

A review of 25 years of the social interaction test

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

A familial unbalanced subtelomeric translocation resulting in monosomy 6q27-->qter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

TATA-binding protein in neurodegenerative disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Microdissection and reverse painting reveals a microdeletion 6(q26qter) in a de novo r(6) chromosome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Transcriptional control of cognitive development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

RNA polymerase II transcription in murine cells lacking the TATA binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

Altered anxiety-related and social behaviors in the Fmr1 knockout mouse model of fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201674

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.EJHG.5201674

1 reference

Dimensions Publication ID

14 October 2017

1026163998

0 references

1 reference