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MYH7 Genotype--Phenotype Correlation in a Cohort of Finnish Patients.
- Published in:
- Cardiogenetics, 2022, v. 12, n. 1, p. 122, doi. 10.3390/cardiogenetics12010013
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- Article
The rare Costello variant HRAS c.173C>T (p.T58I) with severe neonatal hypertrophic cardiomyopathy.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 6, p. 1433, doi. 10.1002/ajmg.a.37596
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- Article
Prevalence and outcomes of finnish MYH7 patients.
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- Cardiology in the Young, 2022, v. 32, p. S129
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Prevalence and outcomes of finnish MYH7 patients.
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- Cardiology in the Young, 2022, v. 32, n. S2, p. S129, doi. 10.1017/S1047951122001950
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- Article
Dielectric and photoluminescence properties of Nd and Ga codoped-BaTiO, prepared by sol-gel method.
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- Journal of Materials Science: Materials in Electronics, 2016, v. 27, n. 11, p. 11371, doi. 10.1007/s10854-016-5262-2
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- Article
Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency.
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- Journal of Inherited Metabolic Disease, 2022, v. 45, n. 2, p. 264, doi. 10.1002/jimd.12462
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- Article
A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia.
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- Human Molecular Genetics, 2010, v. 19, n. 7, p. 1379, doi. 10.1093/hmg/ddq009
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- Article
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations.
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- Human Molecular Genetics, 2009, v. 18, n. 14, p. 2719, doi. 10.1093/hmg/ddp204
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- Article