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Paternal and maternal mutations in X-STRs: A GHEP-ISFG collaborative study.
Pinto N, Pereira V, Tomas C, Loiola S, Carvalho EF, Modesti N, Maxzud M, Marcucci V, Cano H, Cicarelli R, Januario B, Bento A, Brito P, Burgos G, Paz-Cruz E, Díez-Juárez L, Vannelli S, Pontes ML, Berardi G, Furfuro S, Fernandez A, Sumita D, Bobillo C, García MG, Gusmão L. Pinto N, et al. Among authors: cano h. Forensic Sci Int Genet. 2020 May;46:102258. doi: 10.1016/j.fsigen.2020.102258. Epub 2020 Feb 5. Forensic Sci Int Genet. 2020. PMID: 32066109
Detection of a novel 16.3 variant allele at locus DYS533 in R1b males inhabiting southern South America: A 19-nucleotide insertion explains its origin based on Sanger sequencing results.
Sala A, Marino M, Guinudinik A, Marcucci V, Cano H, Rey SV, Bobillo C, Castagnola J, Garrigós-Calivares L, Ginart S, Caputo M, Corach D. Sala A, et al. Among authors: cano h. Forensic Sci Int Genet. 2023 Jan;62:102789. doi: 10.1016/j.fsigen.2022.102789. Epub 2022 Oct 10. Forensic Sci Int Genet. 2023. PMID: 36252401
Diagnosis features of pediatric Gaucher disease patients in the era of enzymatic therapy, a national-base study from the Spanish Registry of Gaucher Disease.
Andrade-Campos M, Alfonso P, Irun P, Armstrong J, Calvo C, Dalmau J, Domingo MR, Barbera JL, Cano H, Fernandez-Galán MA, Franco R, Gracia I, Gracia-Antequera M, Ibañez A, Lendinez F, Madruga M, Martin-Hernández E, O'Callaghan MDM, Del Soto AP, Del Prado YR, Sancho-Val I, Sanjurjo P, Pocovi M, Giraldo P. Andrade-Campos M, et al. Among authors: cano h. Orphanet J Rare Dis. 2017 May 3;12(1):84. doi: 10.1186/s13023-017-0627-z. Orphanet J Rare Dis. 2017. PMID: 28468677 Free PMC article.
20 results