Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study-Reference-Cited by-同舟云学术

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Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study

Published:2012-04-19 Issue:7 Volume:54 Page:618-623
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

DALE RUSSELL C,GRATTAN-SMITH PADRAIC,NICHOLSON MICHELLE,PETERS GREG B

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.2012.04287.x/fullpdf

Reference17 articles.

1. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am J Hum Genet,2010

2. Association between microdeletion and microduplication at 16p11.2 and autism;Weiss;N Engl J Med,2008

3. Myoclonus-dystonia: significance of large SGCE deletions;Grunewald;Hum Mutat,2008

4. New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes;Devos;Mov Disord,2006

5. The monogenic primary dystonias;Muller;Brain,2009

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1. Long‐read sequencing and optical genome mapping identify causative gene disruptions in noncoding sequence in two patients with neurologic disease and known chromosome abnormalities;American Journal of Medical Genetics Part A;2024-07-23

2. Long-term low-dose lamotrigine for paroxysmal kinesigenic dyskinesia: a two-year investigation of cognitive function in children;Frontiers in Psychiatry;2024-03-11

3. Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature;Movement Disorders Clinical Practice;2023-03-16

4. Construction of copy number variation landscape and characterization of associated genes in a Bangladeshi cohort of neurodevelopmental disorders;Frontiers in Genetics;2023-03-07

5. The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders;Movement Disorders;2022-08-25

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