Feliciano J. Ramos
Universidad de Zaragoza
58 papers found
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Severe infantile-onset cardiomyopathy associated with a homozygous deletion in desmin
Download from www.ncbi.nlm.nih.govAntisense therapeutics for neurofibromatosis type 1 caused by deep intronic mutations
UploadTen novelHMGCLmutations in 24 patients of different origin with 3-hydroxy-3-methyl-glutaric aciduria
Download from www.researchgate.netMolecular genetics of HMG-CoA lyase deficiency
Download from www.researchgate.netIncreased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST)
Download from academic.oup.comDetection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles
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