The impact of chromosomal microarray on clinical management: a retrospective analysis.
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Parents' Attitudes toward Clinical Genetic Testing for Autism Spectrum Disorder-Data from a Norwegian Sample.The clinical impact of chromosomal microarray on paediatric care in Hong Kong.Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.Capturing the clinical utility of genomic testing: medical recommendations following pediatric microarrayComparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disordersTen new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A.Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions.Low Rates of Genetic Testing in Children With Developmental Delays, Intellectual Disability, and Autism Spectrum Disorders.Pre- and post-test genetic counseling for chromosomal and Mendelian disorders.CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdensClinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental DisordersGenomic findings in patients with clinical suspicion of 22q11.2 deletion syndrome."Set in Stone" or "Ray of Hope": Parents' Beliefs About Cause and Prognosis After Genomic Testing of Children Diagnosed with ASD.Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability.Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.Identification of EPCAM mutation: clinical use of microarray.Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.Pathways from autism spectrum disorder diagnosis to genetic testing.Clinical performance of the CytoScan Dx Assay in diagnosing developmental delay/intellectual disability.Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray.Quo Vadis clinical genomics of ASD?Genomics in neurodevelopmental disorders: an avenue to personalized medicine
P2860
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P2860
The impact of chromosomal microarray on clinical management: a retrospective analysis.
description
2014 nî lūn-bûn
@nan
2014年の論文
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2014年学术文章
@wuu
2014年学术文章
@zh
2014年学术文章
@zh-cn
2014年学术文章
@zh-hans
2014年学术文章
@zh-my
2014年学术文章
@zh-sg
2014年學術文章
@yue
2014年學術文章
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name
The impact of chromosomal microarray on clinical management: a retrospective analysis.
@en
The impact of chromosomal microarray on clinical management: a retrospective analysis.
@nl
type
label
The impact of chromosomal microarray on clinical management: a retrospective analysis.
@en
The impact of chromosomal microarray on clinical management: a retrospective analysis.
@nl
prefLabel
The impact of chromosomal microarray on clinical management: a retrospective analysis.
@en
The impact of chromosomal microarray on clinical management: a retrospective analysis.
@nl
P2093
P2860
P356
P6366
P1433
P1476
The impact of chromosomal microarray on clinical management: a retrospective analysis.
@en
P2093
Carolyn D Applegate
Denise A S Batista
Elizabeth Wohler
Julie Hoover-Fong
Lindsay B Henderson
Molly B Sheridan
P2860
P2888
P304
P356
10.1038/GIM.2014.18
P407
P577
2014-03-13T00:00:00Z
P6366
2078781148