Rogelio González Sarmiento-rekin lankidetzan egindako argitalpenak (7)

2011

  1. A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism

    Clinical Endocrinology

2010

  1. Analysis of thyroglobulin gene polymorphisms in patients with autoimmune thyroiditis

    Endocrine, Vol. 37, Núm. 3, pp. 389-395

2005

  1. A new case of congenital goiter with hypothyroidism caused by a homozygous p.R277X mutation in the exon 7 of the thyroglobulin gene: A mutational hot spot could explain the recurrence of this mutation

    Journal of Clinical Endocrinology and Metabolism, Vol. 90, Núm. 6, pp. 3766-3770

  2. Study of AZF regions of Y chromosome in males with idiopathic infertility. Analysis of two methods of molecular diagnosis

    Medicina Clinica, Vol. 125, Núm. 19, pp. 731-733

2002

  1. Caso clínico varón de 36 años con ginecomastia

    Medicine: Programa de Formación Médica Continuada Acreditado, Vol. 8, Núm. 82, pp. 4451-4452

2001

  1. Monoallelic deletion in the 5′ region of the thyroglobulin gene as a cause of sporadic nonendemic simple goiter

    Thyroid, Vol. 11, Núm. 8, pp. 789-793

1996

  1. Thyroglobulin exon 10 gene point mutation in a patient with endemic goiter

    Thyroid, Vol. 6, Núm. 5, pp. 423-427