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The Lancet, ISSN 0140-6736, 02/2019, Volume 393, Issue 10173, pp. 719 - 721
In the early 2000s, microarray technology enabled access to submicroscopic CNVs,3–5 and discoveries over the subsequent decade demonstrated the clinical... 
CHROMOSOMAL MICROARRAY | MEDICINE, GENERAL & INTERNAL | Nucleotide sequence | Fetuses | Genes | Genomics | Abnormalities | Disorders | Amino acid sequence | Genomes | Genetic diversity | Neurodevelopmental disorders | Genetic screening | Gene sequencing | Pregnancy | Proteins | Studies | Design | Ultrasonic imaging | DNA microarrays | Transition points | Technology | Coding | Mutation | Anomalies
Journal Article
Neuron, ISSN 0896-6273, 09/2015, Volume 87, Issue 6, pp. 1215 - 1233
Journal Article
Cell Stem Cell, ISSN 1934-5909, 11/2014, Volume 15, Issue 5, pp. 643 - 652
Journal Article
Journal Article
Cell, ISSN 0092-8674, 04/2012, Volume 149, Issue 3, pp. 525 - 537
Journal Article
Cell, ISSN 0092-8674, 12/2016, Volume 167, Issue 7, pp. 1705 - 1718.e13
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2019, Volume 1885, pp. 251 - 265
Precise tests for genomic structural variation (SV) are essential for accurate diagnosis of prenatal genome abnormalities. The two most ubiquitous traditional... 
Copy-number variation | Chromosomal abnormalities | Jumping libraries | Prenatal diagnosis | Whole-genome sequencing | Structural variation
Journal Article
Proceedings of the National Academy of Sciences, ISSN 0027-8424, 10/2014, Volume 111, Issue 42, pp. E4468 - E4477
Journal Article