Found: 9
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Novel mutations in scavenger receptor BI associated with high HDL cholesterol in humans.
- Published in:
- Clinical Genetics, 2011, v. 79, n. 6, p. 575, doi. 10.1111/j.1399-0004.2011.01682.x
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- Publication type:
- Article
ALAS, our frailty is the cause ... of a new for form of protoporphyria.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 1, p. 39, doi. 10.1111/j.1399-0004.2008.01139_1.x
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- Publication type:
- Article
Cilia get serious: Meckel–Gruber and Bardet–Biedl syndromes represent a spectrum of allelic disorders.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 1, p. 40, doi. 10.1111/j.1399-0004.2008.01139_2.x
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- Publication type:
- Article
LeaPIN’ toward the cause of myoglobinuria in childhood.
- Published in:
- Clinical Genetics, 2009, v. 75, n. 1, p. 41, doi. 10.1111/j.1399-0004.2008.01139_3.x
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- Publication type:
- Article
Common inactivating mutations in PCSK9 cause low LDL cholesterol.
- Published in:
- 2005
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- Publication type:
- Other
Hotspot MEF2A at the heart of coronary artery disease?
- Published in:
- 2004
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- Publication type:
- Other
Pharmacogenomic diversity in Singaporean populations and Europeans.
- Published in:
- Pharmacogenomics Journal, 2014, v. 14, n. 6, p. 555, doi. 10.1038/tpj.2014.22
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- Publication type:
- Article
Higher frequency of genetic variants conferring increased risk for ADRs for commonly used drugs treating cancer, AIDS and tuberculosis in persons of African descent.
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- Pharmacogenomics Journal, 2014, v. 14, n. 2, p. 160, doi. 10.1038/tpj.2013.13
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- Publication type:
- Article
Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin.
- Published in:
- Pharmacogenomics Journal, 2012, v. 12, n. 3, p. 233, doi. 10.1038/tpj.2010.92
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- Publication type:
- Article