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103. Whole-exome sequencing in the molecular diagnosis of individuals with congenital anomalies of the kidney and urinary tract and identification of a new causative gene

105. Divergent Levels of Marker Chromosomes in an hiPSC-Based Model of Psychosis

106. Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort

107. Mechanisms for Complex Chromosomal Insertions

108. MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death

109. Identification of a RAI1-associated disease network through integration of exome sequencing, transcriptomics, and 3D genomics

110. Recurrent De Novo and Biallelic Variation of ATAD3A , Encoding a Mitochondrial Membrane Protein, Results in Distinct Neurological Syndromes

112. Exome sequencing in mostly consanguineous Arab families with neurologic disease provides a high potential molecular diagnosis rate

115. Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation inLEMD2, and is associated with sudden cardiac death

116. Nonrecurrent 17p11.2p12 Rearrangement Events that Result in Two Concomitant Genomic Disorders: The PMP22-RAI1 Contiguous Gene Duplication Syndrome

118. Nanoparticle delivery of stable miR-199a-5p agomir improves the osteogenesis of human mesenchymal stem cells via the HIF1a pathway

119. Review and prospect of translational medicine in China

120. Anatomical versus non-anatomical resection for solitary hepatocellular carcinoma without macroscopic vascular invasion: A propensity score matching analysis.

122. Regulation and action of miRNA-199a in health and diseases.

124. Lanthanide triflates catalyze Mn(III)-based oxidative radical cyclization reactions. Enantioselective synthesis of (-)-triptolide, (-)-triptonide, and (+)-triptophenolide

129. Hutterite-type cataract maps to chromosome 6p21.32-p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death.

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