Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report. [PDF]
Siracusano M +5 more
europepmc +1 more source
A European Multicenter Outcome Study of Perioperative Airway Management Policies following Midface Surgery in Syndromic Craniosynostosis. [PDF]
Cuperus IE +24 more
europepmc +1 more source
Molecular analysis of exon 7 of the fibroblast growth factor receptor 2 (FGFR2) gene in an Indonesian patient with Apert syndrome: a case report. [PDF]
Brajadenta GS +4 more
europepmc +1 more source
Apert syndrome: a case report. [PDF]
Khan S, Chatra L, Shenai P, Veena K.
europepmc +1 more source
A 37-year-old Nigerian woman with Apert syndrome - medical and psychosocial perspectives: a case report. [PDF]
Kana MA +3 more
europepmc +1 more source
A longitudinal study of the role of fingers in the development of early number and arithmetic skills in children with Apert syndrome. [PDF]
Hilton C.
europepmc +1 more source
Alternative Methods for Nasotracheal Intubation and Extubation in a Patient With Apert Syndrome. [PDF]
Tsukamoto M, Yokoyama T.
europepmc +1 more source
Novel GLI3 variant causing overlapped Greig cephalopolysyndactyly syndrome (GCPS) and Pallister-Hall syndrome (PHS) phenotype with agenesis of gallbladder and pancreas. [PDF]
Ito S +6 more
europepmc +1 more source
Annotating cancer variants and anti-cancer therapeutics in reactome. [PDF]
Milacic M +7 more
europepmc +1 more source
A novel missense variant in the GLI3 zinc finger domain in a family with digital anomalies. [PDF]
Crapster JA +3 more
europepmc +1 more source

