Associated Papers
Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.
Li Y et al.
Molecular Medicine Reports, 2020
32705272 (PubMed )
Supplement: Supplementary_Data1.xlsx › filter_by_duplicate
Effect for Human Genomic Variation During the BMP4-Induced Conversion From Pluripotent Stem Cells to Trophoblast.
Li HT et al.
Frontiers in Genetics, 2020
32318089 (PubMed )
Supplement: Data_Sheet_1.XLSX › MRucR_annotation
DNA polymorphisms of lipase related genes.
Cao H et al.
Journal of Human Genetics, 2003
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