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Molecular Genetics & Genomic Medicine|December 27, 2019
Forensic characteristics and genetic affinity analyses of Xinjiang Mongolian group using a novel six fluorescent dye-labeled typing system including 41 Y-STRs and 3 Y-InDelsYanfang Liu, Tingting Yu, Shuyan Mei, et al.
Molecular Genetics & Genomic Medicine|December 27, 2019
Novel VAC14 variants identified in two Chinese siblings with childhood-onset striatonigral degenerationShuang Liao, Tingting Chen, Ying Dai, et al.
Molecular Genetics & Genomic Medicine|January 1, 2020
Superoxide imbalance triggered by Val16Ala-SOD2 polymorphism increases the risk of depression and self-reported psychological stress in free-living elderly peopleIvo Emilio da Cruz Jung, Ivana Beatrice Mânica da Cruz, Fernanda Barbisan, et al.
Molecular Genetics & Genomic Medicine|December 12, 2019
MiR-338 regulates NFATc1 expression and inhibits the proliferation and epithelial-mesenchymal transition of human non-small-cell lung cancer cellsWei He, Jibin Lu
Molecular Genetics & Genomic Medicine|February 23, 2018
Consumer use and response to online third-party raw DNA interpretation servicesCatharine Wang, Tiernan J Cahill, Andrew Parlato, et al.
Molecular Genetics & Genomic Medicine|July 19, 2017
A novel molecular diagnostics platform for somatic and germline precision oncologyRubén Cabanillas, Marta Diñeiro, David Castillo, et al.
Molecular Genetics & Genomic Medicine|February 15, 2018
Familial aortic disease and a large duplication in chromosome 16p13.1Philipp Erhart, Tobias Brandt, Beate K Straub, et al.
Molecular Genetics & Genomic Medicine|November 24, 2017
Newborn genetic screening for spinal muscular atrophy in the UK: The views of the general populationFelicity K Boardman, Chloe Sadler, Philip J Young
Molecular Genetics & Genomic Medicine|January 21, 2023
Analysis of ASS1 gene in ten unrelated middle eastern families with citrullinemia type 1 identifies rare and novel variantsMelissa Daou, Mirna Souaid, Tony Yammine, et al.
Molecular Genetics & Genomic Medicine|January 23, 2023
A novel variant in BCL11B in an individual with neurodevelopmental delay: A case reportYonglin Yu, Xiaoyi Jia, Hongwei Yin, et al.
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