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Molecular Genetics & Genomic Medicine|January 3, 2019
Association of human leukocyte antigens-DQB2/DPA1/DPB1 polymorphism and pulmonary tuberculosis in the Chinese Uygur populationXue Wang, Xudong Cao, Wanjiang Zhang, et al.
Molecular Genetics & Genomic Medicine|December 15, 2018
Identification of a de novo splicing variant in the Coffin-Siris gene, SMARCE1, in a patient with Angelman-like syndromeCinthia Aguilera, Elisabeth Gabau, Steve Laurie, et al.
Molecular Genetics & Genomic Medicine|December 15, 2018
The -44 C/G (rs1800972) polymorphism of the β-defensin 1 is associated with increased risk of developing type 2 diabetes mellitusMarco Antonio Martinez-Rios, Gilberto Vargas-Alarcon, Marco Antonio Peña-Duque, et al.
Molecular Genetics & Genomic Medicine|December 18, 2018
Identification of genes associated with cancer progression and prognosis in lung adenocarcinoma: Analyses based on microarray from Oncomine and The Cancer Genome Atlas databasesWei Liu, Songyun Ouyang, Zhigang Zhou, et al.
Molecular Genetics & Genomic Medicine|December 18, 2018
Cancer genetics program: Follow-up on clinical genetics and genomic medicine in QatarSalha Bujassoum Al-Bader, Reem Alsulaiman, Hekmet Bugrein, et al.
Molecular Genetics & Genomic Medicine|November 13, 2019
Association of single nucleotide polymorphisms at 20q12 with nonsyndromic cleft lip with or without cleft palate in a Southern Chinese Han cohortYunpu He, Liheng Huang, Yuqian Zheng, et al.
Molecular Genetics & Genomic Medicine|November 15, 2019
Variant analysis of PEX11B gene from a family with peroxisome biogenesis disorder 14B by whole exome sequencingYuan Tian, Linlin Zhang, Ying Li, et al.
Molecular Genetics & Genomic Medicine|November 17, 2019
DDAH1 promoter -396 4N insertion variant is associated with increased risk of type 2 diabetes in a gender-dependent mannerFasheng Zhu, Chi Zhou, Zheng Wen, et al.
Molecular Genetics & Genomic Medicine|November 29, 2019
Diagnostic accuracy of midkine for hepatocellular carcinoma: A meta-analysisYu Zhang, Juan Tang, Xiao Zhou, et al.
Molecular Genetics & Genomic Medicine|November 29, 2019
Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophyWen-Jiao Luo, Qiao Wei, Hai-Lin Dong, et al.
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