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Frontiers in Cardiovascular Medicine|June 17, 2017
A Path to Implement Precision Child Health Cardiovascular MedicineMarlin Touma, Brian Reemtsen, Nancy Halnon, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 8, 2008
Genetically defined EWS/FLI1 model system suggests mesenchymal origin of Ewing's family tumorsGary Potikyan, Kelly A France, Marc R J Carlson, et al.
BMC Cancer|September 20, 2008
Expression profile of CREB knockdown in myeloid leukemia cellsMatteo Pellegrini, Jerry C Cheng, Jon Voutila, et al.
American Journal of Medical Genetics. Part A|February 7, 2014
X chromosome exome sequencing reveals a novel ALG13 mutation in a nonsyndromic intellectual disability family with multiple affected male siblingsNesrine Bissar-Tadmouri, Whithey L Donahue, Lihadh Al-Gazali, et al.
Molecular Genetics and Metabolism Reports|April 14, 2020
Genetic characterization and long-term management of severely affected siblings with intellectual developmental disorder with cardiac arrhythmia syndromeShahram Yazdani, Anish Badjatiya, Naghmeh Dorrani, et al.
Annals of Neurology|July 17, 2016
Truncating mutations in APP cause a distinct neurological phenotypeSteven Klein, Alexander Goldman, Hane Lee, et al.
Nucleic Acids Research|April 3, 2012
Identification of allele-specific alternative mRNA processing via transcriptome sequencingGang Li, Jae Hoon Bahn, Jae-Hyung Lee, et al.
Plos One|January 5, 2010
Disease gene characterization through large-scale co-expression analysisAllen Day, Jun Dong, Vincent A Funari, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 11, 2014
Assessing the necessity of confirmatory testing for exome-sequencing results in a clinical molecular diagnostic laboratorySamuel P Strom, Hane Lee, Kingshuk Das, et al.
Biomolecular Engineering|April 10, 2003
Evaluation of techniques using amplified nucleic acid probes for gene expression profilingMehrnoosh Saghizadeh, Donald J Brown, Jian Tajbakhsh, et al.
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