PABLO ROMÁN NARANJO VARELA-rekin lankidetzan egindako argitalpenak (3)

2023

  1. A systematic review on machine learning approaches in the diagnosis and prognosis of rare genetic diseases

    Journal of Biomedical Informatics, Vol. 143

2022

  1. A novel nonsense variant in the CENPP gene segregates in a Swiss family with autosomal dominant low-frequency sensorineural hearing loss

    European Journal of Human Genetics, Vol. 30, Núm. 11, pp. 1301-1305

  2. Defective α‐tectorin may involve tectorial membrane in familial Meniere disease

    Clinical and Translational Medicine