Associated Papers
Genetic analysis and prenatal diagnosis of short-rib thoracic dysplasia 3 with or without polydactyly caused by compound heterozygous variants of DYNC2H1 gene in four Chinese families.
Fang Y et al.
Frontiers in Genetics, 2023
37007936 (PubMed )
Supplement: Table2.XLSX › Sheet1
Identification of potential causal variants for premature ovarian failure by whole exome sequencing.
Jin H et al.
Bmc Medical Genomics, 2020
33109206 (PubMed )
Supplement: 12920_2020_813_MOESM1_ESM.xlsx › Table_S4
Identification of Characteristic Genomic Markers in Human Hepatoma HuH-7 and Huh7.5.1-8 Cell Lines.
Kawamoto M et al.
Frontiers in Genetics, 2020
33193621 (PubMed )
Supplement: Data_Sheet_1.xlsx › Candidate_Gene_Detail
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