Found: 5
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Genotype–phenotype association in alpha-thalassemia cohort in a population with high prevalence of alpha and beta-thalassemia: importance of genetic screening.
- Published in:
- Middle East Journal of Medical Genetics, 2021, v. 10, n. 1, p. 1
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- Article
Alzheimer's Disease-Related Epigenetic Changes: Novel Therapeutic Targets.
- Published in:
- Molecular Neurobiology, 2024, v. 61, n. 3, p. 1282, doi. 10.1007/s12035-023-03626-y
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- Article
The association of MMUT mutation (NM_000255.4:c.976A>G) with wide spectrum clinical manifestations in a child affected with methylmalonic acidemia.
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- New Zealand Journal of Medical Laboratory Science, 2023, v. 77, n. 2, p. 75
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- Article
A broad spectrum manifestation in a case affected by 3q29 microdeletion syndrome: a literature review and in silico analysis.
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- New Zealand Journal of Medical Laboratory Science, 2022, v. 76, n. 3, p. 157
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- Article
Genetic variations in IKZF3, LET7‐a2, and CDKN2B‐AS1: Exploring associations with metabolic syndrome susceptibility and clinical manifestations.
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- Journal of Clinical Laboratory Analysis, 2024, v. 38, n. 1/2, p. 1, doi. 10.1002/jcla.24999
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- Article