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Molecular Cytogenetics|May 13, 2024
Efficiency of copy number variation sequencing combined with karyotyping in fetuses with congenital heart disease and the following outcomesXuezhen Wang, Jing Sha, Yu Han, et al.
Molecular Cytogenetics|November 4, 2022
Haploinsufficiencies of FOXF1, FOXC2 and FOXL1 genes originated from deleted 16q24.1q24.2 fragment related with alveolar capillary dysplasia with misalignment of pulmonary veins and lymphedema-distichiasis syndrome: relationship to phenotypeXuezhen Wang, Lili Guo, Bei Zhang, et al.
Risk Management and Healthcare Policy|August 30, 2022
Association Between NLR and NAFLD in Adults Exposed to Famine in Early LifeYing Liu, Zhifang Zhong, Zhihong Li, et al.
Medicine|October 12, 2022
A fetus with Bosch-Boonstra-Schaaf optic atrophy syndrome characterized by bilateral ventricle widening: A case report and related literature reviewYu Sun, Lili Guo, Jing Sha, et al.
Archiv Der Pharmazie|November 30, 2023
Synthesis and activity of arylcoumarin derivatives with therapeutic effects on diabetic nephropathyYinbo Pan, Min Zhou, Zhenzhen Liu, et al.
Frontiers in Genetics|July 17, 2024
Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1Xinrong Zhang, Jiebin Wu, Jianteng Zhou, et al.
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