Found: 6
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Novel Marfan Syndrome-Associated Mutation in the FBN1 Gene Caused by Parental Mosaicism and Leading to Abnormal Limb Patterning.
- Published in:
- Molecular Syndromology, 2017, v. 8, n. 3, p. 148, doi. 10.1159/000467909
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- Article
Increased peripartum mortality associated with maternal subclinical malaria in Mozambique.
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- Malaria Journal, 2023, v. 22, n. 1, p. 1, doi. 10.1186/s12936-023-04613-3
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- Article
CYP2C19 or CYP3A5 Genotyping Does Not Predict Clinical Response to Clopidogrel.
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- Journal of Clinical Pharmacology, 2018, v. 58, n. 10, p. 1274, doi. 10.1002/jcph.1144
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- Article
Wilson disease: revision of diagnostic criteria in a clinical series with great genetic homogeneity.
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- Journal of Gastroenterology, 2021, v. 56, n. 1, p. 78, doi. 10.1007/s00535-020-01745-0
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- Article
Positive clinical response to clopidogrel is independent of paraoxonase 1 Q192R and CYP2C19 genetic variants.
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- Journal of Clinical Pharmacology, 2014, v. 54, n. 8, p. 843, doi. 10.1002/jcph.275
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- Article
Positive Clinical Response to Clopidogrel IS Independent of Paraoxonase 1 Q192R and CYP2C19 Genetic Variants.
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- Journal of Clinical Pharmacology, 2014, v. 54, n. 2, p. 1, doi. 10.1002/jcph.275
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- Article