Results 81 to 90 of about 376 (181)

Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice. [PDF]

Laryngoscope, 2021
Lam AS, Liu CC, Deutsch GH, Rivera J, Perkins JA, Holmes G, Jabs EW, Cunningham ML, Dahl JP.   +8 more
europepmc   +1 more source

Improving medical care for adults with complex rare genetic syndromes:A multidisciplinary approach [PDF]

, 2023
Rosenberg, Anna
core  

[Acrocephalosyndactylia--Apert's syndrome].

Lijecnicki vjesnik, 1968
I, Jelicić, D, Montani, I, Prpić
openaire   +1 more source

Syndromic Craniosynostosis [PDF]

, 2021
Florisson, J.M.G. (Joyce)
core   +1 more source

Apert syndrome: Be aware of the 'dodgy' hip! [PDF]

BMJ Case Rep, 2018
Khan SA, Moores TS, Docker C.
europepmc   +1 more source

Olfactory bulb and olfactory tract abnormalities in acrocallosal syndrome and Greig cephalopolysyndactyly syndrome. [PDF]

Pediatr Radiol, 2019
Subramanian S, Soundara Rajan D, Gaesser J, Wen-Ya Lo C, Panigrahy A.   +4 more
europepmc   +1 more source

A European Multicenter Outcome Study of Perioperative Airway Management Policies following Midface Surgery in Syndromic Craniosynostosis. [PDF]

Plast Reconstr Surg
Cuperus IE, Mathijssen IMJ, van Veelen MC, Bouzariouh A, Stubelius I, Kölby L, Lundborg C, Das S, Johnson D, Wall SA, Larysz DF, Dowgierd K, Koszowska M, Schulz M, Gratopp A, Thomale UW, Zafra Vallejo V, Redondo Alamillos M, Ferreras Vega R, Apolito M, Vergnaud E, Paternoster G, Khonsari RH, Workgroup Craniosynostosis, European Reference Network CRANIO.   +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]

J Med Case Rep, 2019
Brajadenta GS, Sari AIP, Nauphar D, Pratamawati TM, Thoreau V.   +4 more
europepmc   +1 more source

Autistic symptoms in Greig cephalopolysyndactyly syndrome: a family case report. [PDF]

J Med Case Rep, 2019
Siracusano M, Riccioni A, Baratta A, Baldi M, Curatolo P, Mazzone L.   +5 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]

J Anat
Hilton C.
europepmc   +1 more source