Issue Date | Title | Author(s) | Source | scopus | WOS | Fulltext/Archive link |
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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 |