Found: 7
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Whole-exome sequencing studies of nonfunctioning pituitary adenomas.
- Published in:
- 2013
- By:
- Publication type:
- journal article
Whole-exome sequencing studies of nonhereditary (sporadic) parathyroid adenomas.
- Published in:
- 2012
- By:
- Publication type:
- journal article
A Mouse Model of Early-Onset Renal Failure Due to a Xanthine Dehydrogenase Nonsense Mutation.
- Published in:
- PLoS ONE, 2012, v. 7, n. 9, p. 1, doi. 10.1371/journal.pone.0045217
- By:
- Publication type:
- Article
A Mouse with an N-Ethyl- N-Nitrosourea (ENU) Induced Trp589Arg Galnt3Mutation Represents a Model for Hyperphosphataemic Familial Tumoural Calcinosis.
- Published in:
- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043205
- By:
- Publication type:
- Article
Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: Evidence from in-situ synchrotron X-ray scattering and backscattered electron imaging.
- Published in:
- Journal of Bone & Mineral Research, 2012, v. 27, n. 4, p. 876, doi. 10.1002/jbmr.1495
- By:
- Publication type:
- Article
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation.
- Published in:
- Journal of Bone & Mineral Research, 2012, v. 27, n. 2, p. 413, doi. 10.1002/jbmr.547
- By:
- Publication type:
- Article
Pyruvate dehydrogenase E3 binding protein deficiency.
- Published in:
- Human Genetics, 2002, v. 110, n. 2, p. 187, doi. 10.1007/s00439-001-0665-3
- By:
- Publication type:
- Article