Craniofacial features resembling frontonasal dysplasia with a tubulonodular interhemispheric lipoma in the adult 3H1 tuft mouse. [PDF]
Fong KS +7 more
europepmc +1 more source
Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. [PDF]
Twigg SR +15 more
europepmc +1 more source
Perioperative Care of a Four-Year-Old Child With Teebi Hypertelorism Syndrome: A Rare Craniofacial Disorder. [PDF]
Abdelhady E, Tobias JD.
europepmc +1 more source
A rare case report of supernumerary nostril in an infant: clinical presentation, surgical management, and literature review. [PDF]
Singh DK, Pandit N, Dhakal I, Yadav AK.
europepmc +1 more source
Positional programs in early murine facial development and their role in human facial shape variability. [PDF]
Murillo-Rincón AP +6 more
europepmc +1 more source
Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice. [PDF]
Fogelgren B +9 more
europepmc +1 more source
miR-383-3p and miR-6951-3p activate cell proliferation through the regulation of genes related to hypertelorism. [PDF]
Iwaya C, Iwata J.
europepmc +1 more source
Necrotizing Enterocolitis Due to Mesenteric Artery Thrombosis in a Patient with Craniofrontonasal Dysplasia: Casual or Causal Association? [PDF]
Serra G +9 more
europepmc +1 more source
Advances in prenatal ultrasound diagnosis of fetal tympanic ring anomalies. [PDF]
Zhang H +5 more
europepmc +1 more source

