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Establishing normal plasma and 24-hour urinary biochemistry ranges in C3H, BALB/c and C57BL/6J mice following acclimatization in metabolic cages.
- Published in:
- Laboratory Animals, 2010, v. 44, n. 3, p. 218, doi. 10.1258/la.2010.009128
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- Publication type:
- Article
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.
- Published in:
- Nature Genetics, 2013, v. 45, n. 1, p. 93, doi. 10.1038/ng.2492
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- Publication type:
- Article
Occurrence and Treatment of Bone Atrophic Non-Unions Investigated by an Integrative Approach.
- Published in:
- PLoS Computational Biology, 2010, v. 6, n. 9, p. 1, doi. 10.1371/journal.pcbi.1000915
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- Publication type:
- Article
Genome-wide study of familial juvenile hyperuricaemic (gouty) nephropathy (FJHN) indicates a new locus, FJHN3, linked to chromosome 2p22.1-p21.
- Published in:
- Human Genetics, 2011, v. 129, n. 1, p. 51, doi. 10.1007/s00439-010-0897-1
- By:
- Publication type:
- Article
MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO).
- Published in:
- 2005
- By:
- Publication type:
- journal article