The role of X-linked genes and copy-number variations (CNVs) in male infertility remains poorly explored. Our previous array-CGH analyses showed three recurrent deletions in Xq exclusively (CNV67) and prevalently (CNV64, CNV69) found in patients. Molecular and clinical characterisation of these CNVs was performed in this study.
Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility / Lo Giacco, D; Chianese, C; Ars, E; Ruiz-Castañé, E; Forti, G; Krausz, C. - In: EJMG. - ISSN 1468-6244. - STAMPA. - 51:(2014), pp. 340-344. [10.1136/jmedgenet-2013-101988]
Recurrent X chromosome-linked deletions: discovery of new genetic factors in male infertility
Chianese, C;Krausz, C
2014
Abstract
The role of X-linked genes and copy-number variations (CNVs) in male infertility remains poorly explored. Our previous array-CGH analyses showed three recurrent deletions in Xq exclusively (CNV67) and prevalently (CNV64, CNV69) found in patients. Molecular and clinical characterisation of these CNVs was performed in this study.
File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in FLORE sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
