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Paper Details

Identification of novel candidate disease genes from de novo exonic copy number variants.
Genome Med
47
2017
-gene, ARGLU1, BPTF, CMA, CNVs, Exon-targeted microarrays, MEIS2, NONO, PSMD12, PTCHD1, SNVs, STK3, TANGO2, TRIP12, X-linked CNVs, X-linked deletion CNVs, autosomal CNVs, autosomes, candidate disease genes, disease genes, disease-associated genes, exon, exon-targeted arrays, exonic, inherited autosomal CNVs, non-, novel, patients, single, single-exon CNVs, single-gene CNVs, variant allele
Author NameAffiliation
Tomasz GambinBaylor College of Medicine
Tomasz GambinInstitute of Computer Science, Warsaw University of Technology
Tomasz GambinInstitute of Mother and Child
Weimin BiBaylor College of Medicine
Weimin Bi
Pengfei LiuBaylor College of Medicine
Pengfei Liu
Zeynep Coban AkdemirBaylor College of Medicine
Yaping YangBaylor College of Medicine
Yaping Yang
Seema R LalaniBaylor College of Medicine
Seema R LalaniBaylor College of Medicine
Seema R Lalani
Arthur L BeaudetBaylor College of Medicine
Arthur L Beaudet
Arthur L BeaudetBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
James R LupskiBaylor College of Medicine
James R LupskiBaylor College of Medicine
James R LupskiTexas Children's Hospital
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