A novel PTCH1 gene mutation in a pediatric patient associated multiple keratocystic odontogenic tumors of the jaws and Gorlin–Goltz syndrome
2016 ◽
Vol 59
(3)
◽
pp. 335
◽
Keyword(s):
2012 ◽
Vol 114
(4)
◽
pp. e128
Keyword(s):
2019 ◽
Vol 4
(4)
◽
pp. 43-48
Keyword(s):
Keyword(s):
2010 ◽
Vol 56
(12)
◽
pp. 730-734
Keyword(s):
2016 ◽
Vol 6
(2)
◽
pp. 93-100
◽
2014 ◽
Vol 26
(4)
◽
pp. 569-575
◽
Keyword(s):