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The Y chromosome-linked copy number variations and male fertility. 2011 C. Krausz ;C. Chianese ; C. Giachini ;E. Guarducci ;I. Laface ; G.Forti
High resolution X chromosome-specific array-CGH detects new CNVs in infertile males. 2012 C. Krausz; C. Giachini; D.L. Giacco; F. Daguin; C. Chianese; E. Ars; E. Ruiz-Castane; G. Forti; E. Rossi
Novel insights into DNA methylation features in spermatozoa: stability and peculiarities. 2012 C. Krausz;J. Sandoval;S. Sayols;C. Chianese;C. Giachini;H. Heyn;M. Esteller
Y-chromosome microdeletions are not associated with SHOX haploinsufficiency. 2013 Chianese C; Lo Giacco D; Tüttelmann F; Ferlin A; Ntostis P; Vinci S; Balercia G; Ars E; Ruiz-Castañé E; Giglio S; Forti G; Kliesch S; Krausz C.
Reply: Y-chromosome microdeletions are not associated with SHOX haploinsufficiency 2014 C. Krausz;C. Chianese;D. Lo Giacco;F. Tuttelmann;A. Ferlin;P. Ntostis;S. Vinci;G. Balercia;E. Ars;E. Ruiz-Castane;S. Giglio;S. Kliesch;G. Forti
Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility 2014 Lo Giacco, D; Chianese, C; Ars, E; Ruiz-Castañé, E; Forti, G; Krausz, C
Genomic changes in spermatozoa of the aging male. 2014 C. Chianese;S. Brilli;C. Krausz
X chromosome-linked CNVs in male infertility: discovery of overall duplication load and recurrent, patient-specific gains with potential clinical relevance. 2014 C. Chianese;A. C. Gunning;C. Giachini;F. Daguin;G. Balercia;E. Ars;D. L. Giacco;E. Ruiz-Castañé;G. Forti;C. Krausz
Aspetti Genetici ed Epigenetici dell'Infertilità Maschile 2015 Chianese, Chiara
Genetics of male infertility: from research to clinic 2015 Krausz, Csilla; Escamilla, Antoni Riera; Chianese, Chiara
Comprehensive investigation in patients affected by sperm macrocephaly and globozoospermia 2015 Chianese, C; Fino, M G; Riera Escamilla, A; López Rodrigo, O; Vinci, S; Guarducci, E; Daguin, F; Muratori, M; Tamburrino, L; Lo Giacco, D; Ars, E; Bassas, L; Costa, M; Pisatauro, V; Noci, I; Coccia, E; Provenzano, A; Ruiz-Castañé, E; Giglio, S; Piomboni, P; Krausz, C
From exome analysis in idiopathic azoospermia to the identification of a high-risk subgroup for occult Fanconi anemia 2019 Krausz, Csilla; Riera-Escamilla, Antoni; Chianese, Chiara; Moreno-Mendoza, Daniel; Ars, Elisabet; Rajmil, Osvaldo; Pujol, Roser; Bogliolo, Massimo; Blanco, Ignacio; Rodríguez, Ines; Badell, Isabel; Ruiz-Castañé, Eduard; Surrallés, Jordi
Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest. 2019 Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C.
gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study 2019 Moreno-Mendoza D.; Casamonti E.; Paoli D.; Chianese C.; Riera-Escamilla A.; Giachini C.; Fino M.G.; Cioppi F.; Lotti F.; Vinci S.; Magini A.; Ars E.; Sanchez-Curbelo J.; Ruiz-Castane E.; Lenzi A.; Lombardo F.; Krausz C.
Corrigendum. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest. 2020 Riera-Escamilla A, Enguita-Marruedo A, Moreno-Mendoza D, Chianese C, Sleddens-Linkels E, Contini E, Benelli M, Natali A, Colpi GM, Ruiz-Castañé E, Maggi M, Baarends WM, Krausz C.
Mostrati risultati da 1 a 15 di 15
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