A new frontonasal dysplasia syndrome associated with deletion of the SIX2 gene. [PDF]
Hufnagel RB +5 more
europepmc +1 more source
BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome. [PDF]
Miller KA +17 more
europepmc +1 more source
Aristaless-Like Homeobox protein 1 (ALX1) variant associated with craniofacial structure and frontonasal dysplasia in Burmese cats. [PDF]
Lyons LA +7 more
europepmc +1 more source
Facial Abnormality (Frontonasal Dysplasia Sequence)
Shweta Anand, Anju Kapoor
openaire +1 more source
Dentofacial and upper airway characteristics of mild and severe class II division 1 subjects [PDF]
Bollhalder, Julia
core +1 more source
A Twist1-regulated distal enhancer crucial for Alx1 gene expression and function during craniofacial development. [PDF]
Huang Y +6 more
europepmc +1 more source
Frontonasal and Frontofacionasal Dysplasias. Case Report
Jenny Ramírez-Gil +4 more
openaire +1 more source
The ALX1 transcription factor acts in the early cranial mesoderm to specify extraocular muscle formation. [PDF]
Iyyanar PPR, Adhikari N, Lan Y, Jiang R.
europepmc +1 more source
A Pattern of Malformations in the First Trimester Ultrasound. [PDF]
Sereno S +5 more
europepmc +1 more source

