Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism
Recurrence of the p.R277X/p.R1511X compound heterozygous mutation in the thyroglobulin gene in unrelated families with congenital goiter and hypothyroidism: haplotype analysis using intragenic thyroglobulin polymorphisms in: Journal of Endocrinology ...
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2020-2021 REPORT
AE&M 63-1 by Sociedade Brasileira de Endocrinologia e Metabologia - Issuu
2020-2021 REPORT
OFFICIAL JOURNAL OF THE BRAZILIAN SOCIETY OF ENDOCRINOLOGY AND METABOLISM
PDF) Y-STRs in Forensic Medicine: DNA Analysis in Semen Samples of Azoospermic Individuals | José Soares-vieira and Jorge Hallak - Academia.edu
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PDF) Identification of a Kupffer cell subset capable of reverting the T cell dysfunction induced by hepatocellular priming
Hector TARGOVNIK | Universidad de Buenos Aires, Buenos Aires | UBA | Faculty of Pharmacy and Biochemistry | Research profile
PDF) Humanized Mouse Models to Evaluate Cancer Immunotherapeutics
Comparative metabolome and transcriptome analyses of the properties of Kluyveromyces marxianus and Saccharomyces yeasts in apple cider fermentation - ScienceDirect
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PDF) Advances and Perspectives in Genetics of Congenital Thyroid Disorders Associated with Thyroglobulin Gene Mutations
