INSTITUTO DE BIOMEDICINA Y GENÉTICA MOLECULAR (IBGM)
Instituto
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Centro de Regulación Genómica
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Centro de Regulación Genómica (4)
2020
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Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairment
Molecular Vision, Vol. 26, pp. 216-225
2017
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GRECOS Project (Genotyping Recurrence Risk of Stroke): The Use of Genetics to Predict the Vascular Recurrence after Stroke
Stroke, Vol. 48, Núm. 5, pp. 1147-1153
2007
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High frequency of germline succinate dehydrogenase mutations in sporadic cervical paragangliomas in Northern Spain: Mitochondrial succinate dehydrogenase structure-function relationships and clinical-pathological correlations
Journal of Clinical Endocrinology and Metabolism, Vol. 92, Núm. 12, pp. 4853-4864
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Spectrum of mutations in the CFTR gene in cystic fibrosis patients of Spanish ancestry
Annals of Human Genetics, Vol. 71, Núm. 2, pp. 194-201