Targeting of C-ROS-1 Activity Using a Controlled Release Carrier to Treat Craniosynostosis in a Preclinical Model of Saethre-Chotzen Syndrome. [PDF]
Camp E +6 more
europepmc +1 more source
RAB23 loss-of-function mutation causes context-dependent ciliopathy in Carpenter syndrome. [PDF]
Leong WY, Tung WL, Wilkie AOM, Hor CHH.
europepmc +1 more source
[Acrocephalosyndactylia--Apert's syndrome].
I, Jelicić, D, Montani, I, Prpić
openaire +1 more source
Apert syndrome: Be aware of the 'dodgy' hip! [PDF]
Khan SA, Moores TS, Docker C.
europepmc +1 more source
Olfactory bulb and olfactory tract abnormalities in acrocallosal syndrome and Greig cephalopolysyndactyly syndrome. [PDF]
Subramanian S +4 more
europepmc +1 more source
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
Apert syndrome: a case report. [PDF]
Khan S, Chatra L, Shenai P, Veena K.
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
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

