Detalhe da pesquisa
1.
FUT2 Variants Confer Susceptibility to Familial Otitis Media.
Am J Hum Genet
; 103(5): 679-690, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30401457
2.
Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees.
Clin Genet
; 95(5): 634-636, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30828794
3.
Identification of Novel Genes and Biological Pathways That Overlap in Infectious and Nonallergic Diseases of the Upper and Lower Airways Using Network Analyses.
Front Genet
; 10: 1352, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-32010199