A new chromosome x exon-specific microarray platform for screening of patients with X-linked disorders. - Wikidata - wikimedia - TriplyDB

A new chromosome x exon-specific microarray platform for screening of patients with X-linked disorders.

A new chromosome x exon-specific microarray platform for screening of patients with X-linked disorders.

http://www.wikidata.org/entity/Q37396260

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A 3-base pair deletion, c.9711_9713del, in DMD results in intellectual disability without muscular dystrophy.Clinical utility of the X-chromosome array.

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A new chromosome x exon-specific microarray platform for screening of patients with X-linked disorders.

http://www.wikidata.org/entity/Q37396260

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 24 September 2009

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

A new chromosome x exon-specif ...... ients with X-linked disorders.

@en

A new chromosome x exon-specif ...... ients with X-linked disorders.

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type

label

A new chromosome x exon-specif ...... ients with X-linked disorders.

@en

A new chromosome x exon-specif ...... ients with X-linked disorders.

@nl

prefLabel

A new chromosome x exon-specif ...... ients with X-linked disorders.

@en

A new chromosome x exon-specif ...... ients with X-linked disorders.

@nl

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JMOLDX.2009.090086

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The Journal of Molecular Diagnostics

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A new chromosome x exon-specif ...... ients with X-linked disorders.

@en

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Arjan P M de Brouwer

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Claude Moraine

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Guy Froyen

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Hans van Bokhoven

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Hans-Hilger Ropers

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Hilde Van Esch

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Jamel Chelly

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Ludmila Kousoulidou

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Philippos C Patsalis

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Stavros Bashiardes

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P2860

Integrated detection and population-genetic analysis of SNPs and copy number variation

A faster circular binary segmentation algorithm for the analysis of array CGH data.

X-linked mental retardation (XLMR): from clinical conditions to cloned genes.

On the probability that a novel variant is a disease-causing mutation.

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.

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

Monogenic causes of X-linked mental retardation.

ZNF674: a new kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation.

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

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562-568

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10.2353/JMOLDX.2009.090086

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