Detalhe da pesquisa
1.
Diagnostic outcomes of exome sequencing in patients with syndromic or non-syndromic hearing loss.
PLoS One
; 13(1): e0188578, 2018.
Artigo
Inglês
| MEDLINE | ID: mdl-29293505
2.
Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis.
Sci Rep
; 7(1): 3715, 2017 06 16.
Artigo
Inglês
| MEDLINE | ID: mdl-28623311