Results 171 to 180 of about 104,371 (225)

Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases. [PDF]

Genet Med Open
Torella A, Morleo M, Spampanato C, Castello R, Zanobio M, Piluso G, Di Letto P, Onore ME, Rahman SI, Musacchia F, Pinelli M, Vitiello G, De Riso G, Selicorni A, Mariani M, Daolio C, Capra V, Scala M, Nardecchia F, Galosi S, Mastrangelo M, Manti F, Milani D, Romano C, Greco D, Ciaccio C, D'Arrigo S, De Laurentiis A, Coppola A, Zollino M, Pasquetti D, L'Erario FF, Tummolo A, Santoro C, Garavelli L, Marini C, Bigoni S, Tirozzi A, Cetrangolo V, Parenti G, Di Bernardo D, Peron A, Maitz S, Accogli A, Cappuccio G, Banfi S, Casari G, Ballabio A, Brunetti-Pierri N, Nigro V, Telethon Undiagnosed Disease Study group.   +50 more
europepmc   +1 more source

Natural selection acting on complex traits hampers the predictive accuracy of polygenic scores in ancient samples. [PDF]

Am J Hum Genet
Añorve-Garibay V, Huerta-Sanchez E, Sohail M, Ortega-Del Vecchyo D.   +3 more
europepmc   +1 more source

Allò essencial per estar viu : el genoma mínim [PDF]

, 2007
Moya, Andrés
core  

Detection of Streptococcus pneumoniae in sterile liquids using real-time PCR (qPCR) in hospitalized patients with suspected invasive pneumococcal disease. [PDF]

Rev Peru Med Exp Salud Publica
Gonzales BE, Mercado EH, Lopez-Briceño M, Durand Vara D, Campos F, Chaparro E, Del Águila O, Castillo ME, Saenz A, Reyes I, Hernandez R, Ochoa TJ.   +11 more
europepmc   +1 more source

A Complex Case of Retinoblastoma Solved by the Combined Approach of Humor/Plasma cfDNA-NGS and LR-WGS. [PDF]

Genes (Basel)
Innamorato S, Basso SL, Belakhdar O, Bruttini M, Fallerini C, Huseynli H, Caccialupi G, Pasquinelli E, Adduci M, Signori G, Arcuri F, Malagnino V, Siciliano MC, Lazzi S, Pesaresi S, Galimberti D, Galluzzi P, De Francesco S, Hadijstillanou T, Pinto AM, Renieri A, Ariani F.   +21 more
europepmc   +1 more source

[Tuberculosis: Analysis of the history and development of multiple antibiotic resistance]. [PDF]

Rev Med Inst Mex Seguro Soc
Jacobo-Delgado YM, De Jesús-González LA, Rivas-Santiago B.   +2 more
europepmc   +1 more source

Congenital Dermal Melanocytosis Exhibited in Two Patients with Hurler Syndrome: Clinical Characterization and Report of a Recurrent <i>IDUA</i> Allele in Colombia. [PDF]

Int J Mol Sci
Vanegas S, Ramírez-Montaño D, Padilla-Guzmán A, Pachajoa H.   +3 more
europepmc   +1 more source

Detection of a <i>bla</i>_KPC-2 carrying IncP-6 plasmid in <i>Aeromonas caviae</i> isolated from a clinical sample in a Spanish hospital. [PDF]

Rev Esp Quimioter
González-Corralejo C, García-Salguero C, Martínez-Rodríguez M, Delgado-Iribarren García-Campero A, Culebras-López E.   +4 more
europepmc   +1 more source

Declaración Universal sobre el Genoma y Derechos Humanos [PDF]

, 1998
Institut Borja de Bioètica,
core  

Gene variants, oxidative stress and inflammation in Colombian populations [PDF]

Biomedica
Banguera DN, Mejía LG, Ramírez-Montano D, Perenguez-Verdugo M, Castillo A.   +4 more
europepmc   +1 more source