Whole exome sequencing in non-obstructive azoospermia allows the identification of a high-risk subgroup of infertile men for undiagnosed Fanconi Anemia, a cancer-prone disease

C. Krausz; A. Riera-Escamilla; C. Chianese; D. Moreno-Mendoza; O. Rajmil; M. Bogliolo; I. Blanco; E. Ars; E. Ruiz-Castane; J. Surralles

Whole exome sequencing in non-obstructive azoospermia allows the identification of a high-risk subgroup of infertile men for undiagnosed Fanconi Anemia, a cancer-prone disease

C. Krausz, A. Riera-Escamilla, C. Chianese, D. Moreno-Mendoza, O. Rajmil, M. Bogliolo, I. Blanco, E. Ars, E. Ruiz-Castane, J. Surralles

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Idioma original	Inglés
Páginas (desde-hasta)	4-4
Número de páginas	1
Publicación	European Journal of Human Genetics
Volumen	27
Estado	Publicada - jul 2019

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Krausz, C., Riera-Escamilla, A., Chianese, C., Moreno-Mendoza, D., Rajmil, O., Bogliolo, M., Blanco, I., Ars, E., Ruiz-Castane, E., & Surralles, J. (2019). Whole exome sequencing in non-obstructive azoospermia allows the identification of a high-risk subgroup of infertile men for undiagnosed Fanconi Anemia, a cancer-prone disease. European Journal of Human Genetics, 27, 4-4.

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Krausz, C, Riera-Escamilla, A, Chianese, C, Moreno-Mendoza, D, Rajmil, O, Bogliolo, M, Blanco, I, Ars, E, Ruiz-Castane, E & Surralles, J 2019, 'Whole exome sequencing in non-obstructive azoospermia allows the identification of a high-risk subgroup of infertile men for undiagnosed Fanconi Anemia, a cancer-prone disease', European Journal of Human Genetics, vol. 27, pp. 4-4.

Whole exome sequencing in non-obstructive azoospermia allows the identification of a high-risk subgroup of infertile men for undiagnosed Fanconi Anemia, a cancer-prone disease. / Krausz, C.; Riera-Escamilla, A.; Chianese, C. et al.
En: European Journal of Human Genetics, Vol. 27, 07.2019, p. 4-4.

Producción científica: Contribución a una revista › Artículo › Investigación › revisión exhaustiva

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