1.
LAMM syndrome: two new patients with a novel mutation in FGF3 gene and additional clinical findings.
Clin Dysmorphol
; 28(2): 81-85, 2019 Apr.
Article
in English
| MEDLINE
| ID: mdl-30433887
Subject(s)
Congenital Microtia/genetics , Ear, Inner/abnormalities , Fibroblast Growth Factor 3/genetics , Hearing Loss, Sensorineural/genetics , Tooth Abnormalities/genetics , Adult , Congenital Microtia/physiopathology , Ear, Inner/physiopathology , Female , Fibroblast Growth Factor 3/physiology , Hearing Loss, Sensorineural/physiopathology , Humans , Mutation , Pedigree , Siblings , Tooth Abnormalities/physiopathology
2.
Turk J Anaesthesiol Reanim
; 42(5): 292-3, 2014 Oct.
Article
in English
| MEDLINE
| ID: mdl-27366440