Found: 8
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Are GJB2 mutations an aggravating factor in the phenotypic expression of mitochondrial non-syndromic deafness?
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 5, p. 265, doi. 10.1038/jhg.2010.23
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- Article
Assessment of Megakaryopoiesis in Children with Acute Lymphoblastic Leukemia.
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- Acta Haematologica, 2005, v. 114, n. 2, p. 91, doi. 10.1159/000086581
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- Article
Pathologic, radiographic and molecular findings in three fetuses diagnosed with HEM/Greenberg skeletal dysplasia.
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- Prenatal Diagnosis, 2008, v. 28, n. 4, p. 309, doi. 10.1002/pd.1976
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- Article
Screening for Congenital Hypothyroidism: The Significance of Threshold Limit in False-Negative Results.
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- Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 9, p. 4283, doi. 10.1210/jc.2010-0057
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- Article
Investigating the impact of the Down syndrome related common MTHFR 677C>T polymorphism in the Danish population.
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- Disease Markers, 2009, v. 27, n. 6, p. 279, doi. 10.1155/2009/725614
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- Article
Melatonin and Immunomodulation: Connections and Potential Clinical Applications.
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- Neuroimmunomodulation, 2006, v. 13, n. 3, p. 133, doi. 10.1159/000097258
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- Article
Erythrocyte membrane Na<sup>+</sup>,K<sup>+</sup>-ATPase and Mg<sup>2+</sup>-ATPase activities in subjects with methylenetetrahydrofolate reductase ( MTHFR) 677 C→T genotype and moderate hyperhomocysteinaemia. The role of L-phenylalanine and L-alanine
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- Clinical Chemistry & Laboratory Medicine, 2006, v. 44, n. 4, p. 423, doi. 10.1515/CCLM.2006.069
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- Article
Erythrocyte membrane acetylcholinesterase activity in subjects with MTHFR 677C?T genotype.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2006, v. 44, n. 1, p. 23, doi. 10.1515/CCLM.2006.005
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- Article