Search Result "aCGH"
Using Free and Open-Source Bioconductor Packages to Analyze Array Comparative Genomics Hybridization (aCGH) Data
Journal: Current Genomics
Volume: 10 Issue: 1 Year: 2009 Page: 60-63
Author(s): Simon Lin, Pan Du, Nadereh Jafari, Toru Ouchi
NeuroArray: A Customized aCGH for the Analysis of Copy Number Variations in Neurological Disorders
Journal: Current Genomics
Volume: 19 Issue: 6 Year: 2018 Page: 431-443
Author(s): Valentina La Cognata,Giovanna Morello,Giulia Gentile,Francesca Cavalcanti,Rita Cittadella,Francesca Luisa Conforti,Elvira Valeria De Marco,Angela Magariello,Maria Muglia,Alessandra Patitucci,Patrizia Spadafora,Velia D`Agata,Martino Ruggieri,Sebastiano Cavallaro
NeuroArray, A Custom CGH Microarray to Decipher Copy Number Variants in Alzheimerâs Disease
Journal: Current Genomics
Volume: 19 Issue: 6 Year: 2018 Page: 499-504
Author(s): Denis Cuccaro,Maria Guarnaccia,Rosario Iemmolo,Velia D`Agata,Sebastiano Cavallaro
DNA Copy Number Profiles Correlate with Outcome in Colorectal Cancer Patients Treated with Fluoropyrimidine/Antifolate-based Regimens
Journal: Current Drug Metabolism
Volume: 12 Issue: 1 Year: 2011 Page: 956-965
Author(s): Leticia G. Leon, Elisa Giovannetti, Kees Smid, Bart P.P. van Houte, Axel R. Hanauske, Giuseppe Giaccone, Godefridus J. Peters
Significance of Genome-Wide Analysis of Copy Number Alterations and UPD in Myelodysplastic Syndromes using Combined CGH â SNP Arrays
Journal: Current Medicinal Chemistry
Volume: 19 Issue: 22 Year: 2012 Page: 3739-3747
Author(s): Ausaf Ahmad,M. Anwar Iqbal
Finding Recurrent Copy Number Alteration Regions: A Review of Methods
Journal: Current Bioinformatics
Volume: 5 Issue: 1 Year: 2010 Page: 1-17
Author(s): Oscar M. Rueda, Ramon Diaz-Uriarte
Structural Chromosome Abnormalities Associated with Obesity: Report of Four New Subjects and Review of Literature
Journal: Current Genomics
Volume: 12 Issue: 3 Year: 2011 Page: 190-203
Author(s): Majed J. Dasouki, Erin L. Youngs, Karine Hovanes
Genetic Testing for Rare Genetic Disorders
Ebook: Omics Technologies for Clinical Diagnosis and Gene Therapy: Medical Applications in Human Genetics
Volume: 1 Year: 2022
Author(s):
Doi: 10.2174/9789815079517122010005
Split Hand Foot Malformation Syndrome: A Novel Heterozygous FGFR1 Mutation Detected by Next Generation Sequencing
Journal: Current Genomics
Volume: 20 Issue: 3 Year: 2019 Page: 226-230
Author(s): âPanayiota Papasozomenou,âIoannis Papoulidis,âThemistoklis Mikos,âMenelaos Zafrakas
Malignant Glioma In Vitro Models: On the Utilization of Stem-like Cells
Journal: Current Cancer Drug Targets
Volume: 17 Issue: 3 Year: 2017 Page: 255-266
Author(s): Rutger K. Balvers,Clemens M.F. Dirven,Sieger Leenstra,Martine L.M. Lamfers