Missense mutation in the MEN1 gene discovered through whole exome sequencing co-segregates with familial hyperparathyroidism.
- Published in:
- Genetics Research, 2013, v. 95, n. 4, p. 114, doi. 10.1017/S0016672313000141
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- Publication type:
- Article
Works matching IS 00166723 AND DT 2013 AND VI 95 AND IP 4
Results: 4
1
2
Let's get real about virtual: online health is here to stay.
- Published in:
- Genetics Research, 2013, v. 95, n. 4, p. 111, doi. 10.1017/S001667231300013X
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- Publication type:
- Article
3
A very rare entity of diabetes insipidus associated with Edwards Syndrome.
- Published in:
- Genetics Research, 2013, v. 95, n. 4, p. 130, doi. 10.1017/S0016672313000165
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- Publication type:
- Article
4
High-throughput sequencing of autism spectrum disorders comes of age.
- Published in:
- Genetics Research, 2013, v. 95, n. 4, p. 121, doi. 10.1017/S0016672313000153
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- Publication type:
- Article