Sporadic male patients with intellectual disability: Contribution of X-chromosome copy number variants-Reference-Cited by-同舟云学术

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Sporadic male patients with intellectual disability: Contribution of X-chromosome copy number variants

Published:2012-11 Issue:11 Volume:55 Page:577-585
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Isrie M.,Froyen G.,Devriendt K.,de Ravel T.,Fryns J.P.,Vermeesch J.R.,Van Esch H.

Funder

Geconcerteerde Onderzoeks Actie

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference60 articles.

1. Genetics and epigenetics of the X-chromosome;Morey;Annals of the New York Academy of Sciences,2010

2. Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium;de Brouwer;Human Mutation,2007

3. X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation;Madrigal;BMC Genomics,2007

4. X chromosome array-CGH for the identification of novel X-linked mental retardation genes;Bauters;European Journal of Medical Genetics,2005

5. Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis;Vissers;Journal of Medical Genetics,2010

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2. X-linked variations inSHROOM4are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems;Journal of Medical Genetics;2022-11-15

3. X-Linked CNV in Pathogenetics of Intellectual Disability;Russian Journal of Genetics;2022-10

4. SHROOM4 Variants Are Associated With X-Linked Epilepsy With Features of Generalized Seizures or Generalized Discharges;Frontiers in Molecular Neuroscience;2022-05-17

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