Associated Papers
Targeted Next-Generation Sequencing Successfully Detects Causative Genes in Chinese Patients with Hereditary Hearing Loss.
Chen S et al.
Genetic Testing and Molecular Biomarkers, 2016
Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.
Ishizuka K et al.
Plos One, 2016
Whole-exome sequencing of primary plasma cell leukemia discloses heterogeneous mutational patterns.
Cifola I et al.
Oncotarget, 2015
26046463 (PubMed )
Supplement: oncotarget-06-17543-s004.xls › Suppl_File_3
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