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A novel frameshift mutation of the endoglin(ENG) gene causes hereditary hemorrhagic telangiectasia in a Chinese family.
- Published in:
- European Archives of Oto-Rhino-Laryngology, 2024, v. 281, n. 1, p. 237, doi. 10.1007/s00405-023-08186-4
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- Article
Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.
- Published in:
- BioMed Research International, 2016, v. 2016, p. 1, doi. 10.1155/2016/1302914
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- Article
Circ_0058124 Upregulates MAPK1 Expression to Promote Proliferation, Metastasis and Metabolic Abilities in Thyroid Cancer Through Sponging miR-940.
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- OncoTargets & Therapy, 2020, v. 13, p. 1569, doi. 10.2147/OTT.S237307
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- Article
Genetically predicted allergic rhinitis causally increases the risk of erectile dysfunction.
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- Frontiers in Genetics, 2024, p. 1, doi. 10.3389/fgene.2024.1423357
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- Article
Identification of a novel missense mutation in the WFS1 gene as a cause of autosomal dominant nonsyndromic sensorineural hearing loss in all-frequencies.
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- American Journal of Medical Genetics. Part A, 2014, v. 164A, n. 12, p. 3052, doi. 10.1002/ajmg.a.36760
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- Article