Detalhe da pesquisa
1.
PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome.
J Hum Genet
; 63(9): 965-969, 2018 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-29930296
2.
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development.
Am J Hum Genet
; 94(1): 23-32, 2014 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-24360809