Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
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Open Access
- 14 May 2010
- journal article
- review article
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 86 (5), 749-764
- https://doi.org/10.1016/j.ajhg.2010.04.006
Abstract
No abstract availableKeywords
This publication has 105 references indexed in Scilit:
- Origins and functional impact of copy number variation in the human genomeNature, 2009
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl ResourcesAmerican Journal of Human Genetics, 2009
- Population Analysis of Large Copy Number Variants and Hotspots of Human Genetic DiseaseAmerican Journal of Human Genetics, 2009
- Large recurrent microdeletions associated with schizophreniaNature, 2008
- Systematic assessment of copy number variant detection via genome-wide SNP genotypingNature Genetics, 2008
- Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal CohortAmerican Journal of Human Genetics, 2008
- The Fine-Scale and Complex Architecture of Human Copy-Number VariationAmerican Journal of Human Genetics, 2008
- A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizuresNature Genetics, 2008
- Structural Variation of Chromosomes in Autism Spectrum DisorderAmerican Journal of Human Genetics, 2008
- Global variation in copy number in the human genomeNature, 2006