Detalhe da pesquisa
1.
Comprehensive phenotypic and functional analysis of dominant and recessive FOXE3 alleles in ocular developmental disorders.
Hum Mol Genet
; 30(17): 1591-1606, 2021 08 12.
Artigo
Inglês
| MEDLINE | ID: mdl-34046667
2.
Hereditary hyperferritinemia-cataract syndrome in three Czech families: molecular genetic testing and clinical implications.
J AAPOS
; 24(6): 352.e1-352.e5, 2020 12.
Artigo
Inglês
| MEDLINE | ID: mdl-33221470