Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Silvia Vannelli"'
Autor:
Andrea Sala, Miguel Marino, Alejandra Guinudinik, Valeria Marcucci, Hortensia Cano, Silvia Vannelli Rey, Cecilia Bobillo, Josefina Castagnola, Lucía Garrigós-Calivares, Santiago Ginart, Mariela Caputo, Daniel Corach
Publikováno v:
Forensic Science International: Genetics. 62:102789
We typed 1541 Y-STR haplotypes from reference samples along forensic casework investigations. In three haplotypes, we detected a variant allele designed as 16.3 at locus DYS533. This was confirmed by amplification using two commercial kits. Sanger se
Autor:
Gabriela Berardi, G. Burgos, Elizeu Fagundes de Carvalho, Mariana K. Maxzud, Hortensia Cano, A.M. Bento, S. Loiola, Regina Maria Barretto Cicarelli, Vania Pereira, Carmen Tomas, Elius Paz-Cruz, Leonor Gusmão, Nádia Pinto, P. Brito, Cecilia Bobillo, Alberto Fernández, Nidia M. Modesti, María Gabriela García, Laura Díez-Juárez, Bianca Januario, Sandra Furfuro, Denilce R. Sumita, Silvia Vannelli, Valeria Cecilia Marcucci, M.L. Pontes
Publikováno v:
Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Made available in DSpace on 2020-12-12T01:14:43Z (GMT). No. of bitstreams: 0 Previous issue date: 2020-05-01 The GHEP-ISFG organized a collaborative study to estimate mutation rates for the markers included in the Investigator Argus X-12 QS kit Qiage
Autor:
Maria Baffico, David J. Bunyan, Emma-Jane Taylor, Adam A. Herridge, Sébastien Schmitt, Antonino Forabosco, Deborah J. Shears, Lorenzo Iughetti, Lucia Capone, Silvia Vannelli, Domenico A. Coviello
Leri-Weill dyschondrosteosis is a pseudoautosomal dominantly-inherited skeletal dysplasia ascribed to haploinsufficiency of the SHOX gene caused by deletions, point mutations, or partial duplications of the gene, or to heterozygous deletions upstream
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d95b5d4af799b1c793b3eb3246d8b921
https://hdl.handle.net/11380/1105029
https://hdl.handle.net/11380/1105029
Autor:
Sala, Andrea, Marino, Miguel, Guinudinik, Alejandra, Marcucci, Valeria, Cano, Hortensia, Rey, Silvia Vannelli, Bobillo, Cecilia, Castagnola, Josefina, Garrigós-Calivares, Lucía, Ginart, Santiago, Caputo, Mariela, Corach, Daniel
Publikováno v:
Forensic Science International: Genetics; Jan2023, Vol. 62, pN.PAG-N.PAG, 1p