Determination of genomic breakpoints in an epileptic patient using genotyping array
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference22 articles.
1. Quantitative mapping of amplicon structure by array CGH identifies CYP24 as a candidate oncogene;Albertson;Nat. Genet.,2000
2. Genomic microarrays in human genetic disease and cancer;Albertson;Hum. Mol. Genet.,2003
3. Quantitative analysis of chromosomal CGH in human breast tumors associates copy number abnormalities with p53 status and patient survival;Jain;Proc. Natl. Acad. Sci. USA,2001
4. High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization;Veltman;Am. J. Hum. Genet.,2002
5. Detection of large-scale variation in the human genome;Iafrate;Nat. Genet.,2004
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1. RBPJ is disrupted in a case of proximal 4p deletion syndrome with epilepsy;Brain and Development;2014-06
2. Microarray Analysis in Children With Developmental Disorder or Epilepsy;Pediatric Neurology;2010-12
3. IS LGI2 THE CANDIDATE GENE FOR PARTIAL EPILEPSY WITH PERICENTRAL SPIKES?;Journal of Bioinformatics and Computational Biology;2010-02
4. Microchromosomal deletions involvingSCN1Aand adjacent genes in severe myoclonic epilepsy in infancy;Epilepsia;2008-09
5. Development of individualized medicine for epilepsy based on genetic information;Expert Review of Clinical Pharmacology;2008-09
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