公開日期 | 標題 | 作者 | 來源出版物 | scopus | WOS | 全文 |
---|---|---|---|---|---|---|
2016 | De novo mutation and somatic mosaicism of gene mutation in type 2A, 2B and 2M VWD | MING-CHING SHEN ; MING CHEN ; Ma G.-C.; Chang S.-P.; Lin C.-Y.; Lin B.-D.; Hsieh H.-N. | Thrombosis Journal | 6 | 0 | |
2018 | Segmental uniparental disomy as a rare cause of congenital severe factor XIII deficiency in a girl with only one heterozygous carrier parent | MING-CHING SHEN ; Chen M.; Chang S.-P.; Lin P.-T.; Hsieh H.-N.; Lin K.-H. | Pediatric Hematology and Oncology | 1 | 0 |