Xenética de Enfermidades Humanas
Fundación Pública Galega de Medicina Xenómica
Santiago de Compostela, EspañaPublicacións en colaboración con investigadores/as de Fundación Pública Galega de Medicina Xenómica (11)
2024
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Bilateral Uveal Melanoma: An Insight into Genetic Predisposition in Four New Unrelated Patients and Review of Published Cases
Journal of Clinical Medicine, Vol. 13, Núm. 11
2023
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Two cases of familial glomuvenous malformation and description of a novel pathogenic mutation in glomulin gene (GLMN)
International Journal of Dermatology
2018
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Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery
Human Mutation, Vol. 39, Núm. 8, pp. 1126-1138
2017
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Autosomal recessive agammaglobulinemia due to defect in μ heavy chain caused by a novel mutation in the IGHM gene
Genes and Immunity, Vol. 18, Núm. 3, pp. 197-199
2013
2011
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LIF, a novel STAT5-regulated gene, is aberrantly expressed in myeloproliferative neoplasms
Genes and Cancer, Vol. 2, Núm. 5, pp. 593-596
2010
2009
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Anagrelide treatment in early pregnancy in a patient with JAK2V617F-positive essential thrombocythemia: Case report and literature review
Acta Haematologica, Vol. 122, Núm. 4, pp. 221-222
2008
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Hypochondroplasia and acanthosis nigricans: A new syndrome due to the p.Lys650Thr mutation in the fibroblast growth factor receptor 3 gene?
European Journal of Endocrinology, Vol. 159, Núm. 3, pp. 243-249
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Serum TNF-α levels in relation to alcohol consumption and common TNF gene polymorphisms
Alcohol, Vol. 42, Núm. 6, pp. 513-518
2006
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Gene by environment interaction: The -159C/T polymorphism in the promoter region of the CD14 gene modifies the effect of alcohol consumption on serum IgE levels
Alcoholism: Clinical and Experimental Research, Vol. 30, Núm. 1, pp. 7-14