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Molecular Genetics & Genomic Medicine|February 12, 2024
Retraction: Forensic characteristics and phylogenetic analyses of one branch of Tai-Kadai language-speaking Hainan Hlai (Ha Hlai) via 23 autosomal STRs included in the Huaxia™ Platinum System
Molecular Genetics & Genomic Medicine|February 12, 2024
Retraction: Evaluation of a six-dye multiplex composed of 27 markers for forensic analysis and databasing
Molecular Genetics & Genomic Medicine|February 10, 2024
Associations of genetic variants within TYK2 with pulmonary tuberculosis among Chinese populationMingwu Zhang, Zhengwei Liu, Yelei Zhu, et al.
Molecular Genetics & Genomic Medicine|February 12, 2024
Retraction: Population genetic analysis of Shaanxi male Han Chinese population reveals genetic differentiation and homogenization of East Asians
Molecular Genetics & Genomic Medicine|February 12, 2024
Retraction: Concordance and characterization of massively parallel sequencing at 58 STRs in a Tibetan population
Molecular Genetics & Genomic Medicine|April 13, 2024
Genotype and phenotype in patients with ACAN gene variants: Three cases and literature reviewWei Tang, Ke-Mi Wu, Qiong Zhou, et al.
Molecular Genetics & Genomic Medicine|February 24, 2024
Type 1 early infantile epileptic encephalopathy: A case report and literature reviewErfan Zaker, Negar Nouri, Mojtaba Movahedinia, et al.
Molecular Genetics & Genomic Medicine|February 26, 2024
Novel variants in TNRC6B cause global developmental delay with speech and behavioral abnormalities, short stature, low body weight, café-au-lait spots, and metabolic abnormalityQi Yang, Shan Ou, Xunzhao Zhou, et al.
Molecular Genetics & Genomic Medicine|February 26, 2024
The first Chinese intellectual developmental disorder, autosomal recessive 57 patient with two novel MBOAT7 variantsHuimin Li, Zhan Qi, Limin Xie, et al.
Molecular Genetics & Genomic Medicine|February 26, 2024
Novel hemizygous single-nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing lossRyan J German, Blake Vuocolo, Liesbeth Vossaert, et al.
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