Found: 10
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The genetic basis of apparently idiopathic ventricular fibrillation: a retrospective overview.
- Published in:
- EP: Europace, 2023, v. 25, n. 11, p. 1, doi. 10.1093/europace/euad336
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- Article
Myo-inositol, glucose and zinc status as risk factors for non-syndromic cleft lip with or without cleft palate in offspring: a case–control study.
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- BJOG: An International Journal of Obstetrics & Gynaecology, 2004, v. 111, n. 7, p. 661, doi. 10.1111/j.1471-0528.2004.00171.x
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- Article
Mutations in PDLIM5 are rare in dilated cardiomyopathy but are emerging as potential disease modifiers.
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- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 2, p. N.PAG, doi. 10.1002/mgg3.1049
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- Article
Growth charts for Marfan syndrome in the Netherlands and analysis of genotype–phenotype relationships.
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- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 2, p. 479, doi. 10.1002/ajmg.a.63047
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- Article
Phenotypic clustering of dilated cardiomyopathy patients highlights important pathophysiological differences.
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- European Heart Journal, 2021, v. 42, n. 2, p. 162, doi. 10.1093/eurheartj/ehaa841
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- Article
The MSX1 allele 4 homozygous child exposed to smoking at periconception is most sensitive in developing nonsyndromic orofacial clefts.
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- Human Genetics, 2008, v. 124, n. 5, p. 525, doi. 10.1007/s00439-008-0569-6
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- Article
The I105V polymorphism in glutathione S-transferase P1, parental smoking and the risk for nonsyndromic cleft lip with or without cleft palate.
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- European Journal of Human Genetics, 2008, v. 16, n. 3, p. 358, doi. 10.1038/sj.ejhg.5201973
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- Article
Maternal dietary B vitamin intake, other than folate, and the association with orofacial cleft in the offspring.
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- European Journal of Nutrition, 2004, v. 43, n. 1, p. 7, doi. 10.1007/s00394-004-0433-y
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- Article
A global longitudinal strain cut-off value to predict adverse outcomes in individuals with a normal ejection fraction.
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- ESC Heart Failure, 2021, v. 8, n. 5, p. 4343, doi. 10.1002/ehf2.13465
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- Article
Hypertrophic remodelling in cardiac regulatory myosin light chain (MYL2) founder mutation carriers.
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- European Heart Journal, 2016, v. 37, n. 23, p. 1815, doi. 10.1093/eurheartj/ehv522
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- Article