Showing results (901-910 of 2,518) with videos related to

Sort By:
Pageof 252
Molecular Genetics & Genomic Medicine|December 14, 2019
Hypomethylation of MIR-378 5'-flanking region predicts poor survival in young patients with myelodysplastic syndromeDe-Hong Wu, Xiao-Wen Zhu, Xiang-Mei Wen, et al.
Molecular Genetics & Genomic Medicine|December 15, 2019
Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformationsJohanna Winberg, Peter Gustavsson, Ellika Sahlin, et al.
Molecular Genetics & Genomic Medicine|January 9, 2020
Modification effect of sex and obesity on the correlation of LEP polymorphisms with leptin levels in Taiwanese obese womenDe-Min Duan, Jing-Yi Jhang, Semon Wu, et al.
Molecular Genetics & Genomic Medicine|January 10, 2020
Novel truncating variant of PPM1D penultimate exon in a Chinese patient with Jansen-de Vries syndromeZhuoguang Li, Caiqi Du, Cai Zhang, et al.
Molecular Genetics & Genomic Medicine|January 22, 2020
Application of targeted panel sequencing and whole exome sequencing for 76 Chinese families with retinitis pigmentosaHandong Dan, Xin Huang, Yiqiao Xing, et al.
Molecular Genetics & Genomic Medicine|January 22, 2020
Copy number variation in DRC1 is the major cause of primary ciliary dyskinesia in the Japanese populationKazuhiko Takeuchi, Yifei Xu, Masako Kitano, et al.
Molecular Genetics & Genomic Medicine|January 22, 2020
Identification of six novel variants in Waardenburg syndrome type II by next-generation sequencingShumin Ren, Xiaojie Chen, Xiangdong Kong, et al.
Molecular Genetics & Genomic Medicine|February 4, 2020
Identification of genes of prognostic value in the ccRCC microenvironment from TCGA databaseBangbei Wan, Bo Liu, Yuan Huang, et al.
Molecular Genetics & Genomic Medicine|February 5, 2020
Genetic diversity and phylogenetic structure of four Tibeto-Burman-speaking populations in Tibetan-Yi corridor revealed by insertion/deletion polymorphismsXing Zou, Guanglin He, Mengge Wang, et al.
Molecular Genetics & Genomic Medicine|December 19, 2019
Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array-based detection rateIlaria Catusi, Maria Paola Recalcati, Ilaria Bestetti, et al.
Pageof 252