| No | 記事 | 記事著者 |
|---|
| 1 | A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass trait | Randall D. Little, et al |
| 2 | Mutations in the proenterpeptidase gene are the molecular cause of congenital enteropeptidase deficiency. | Andreas Holzinger, et al |
| 3 | Molecular and clinical characteristics of MSH6 variant: an analusis of 25 index carriers of a germline variant. | Maran J.W.Berends, et al |
