Book Chapter
Apert Syndrome
2006, Atlas of Genetic Diagnosis and Counseling, Pages 61-69
Book Chapter
Crouzon Syndrome
2006, Atlas of Genetic Diagnosis and Counseling, Pages 261-264
Book Chapter
Crouzon Syndrome
2005, Abnormal Skeletal Phenotypes, Part II, Pages 672-673
Journal Article
Q289P mutation in the FGFR2 gene: first report in a patient with type 1 Pfeiffer syndrome
Maria Piccione, Vincenzo Antona, Marcello Niceta, Carmelo Fabiano and Manuela Martines, et al.
European Journal of Pediatrics, 2009, Volume 168, Number 9, Pages 1135-1139
Book Chapter
Syndromic Craniosynostosis
Francis R. Johns, John A. Jane and Kant Lin
Springer Specialist Surgery Series, 2005, Neurosurgery, VIII, Pages 461-473
Book Chapter
The Neural Crest and Craniofacial Malformations
Hans ten Donkelaar and Christl Vermeij-Keers
2006, Clinical Neuroembryology, Pages 191-228
Book Chapter
Crouzon Syndrome: Basic Dysmorphology and Staging of Reconstruction
Jeffrey C. Posnick
2002, Craniomaxillofacial Reconstructive and Corrective Bone Surgery, Section VI, Pages 713-726
Book Chapter
Pfeiffer Syndrome
2005, Abnormal Skeletal Phenotypes, Part II, Pages 827-829
Book Chapter
Surgical Correction of the Apert Craniofacial Deformities
E. Clyde Smoot and William L. Hickerson
2002, Craniomaxillofacial Reconstructive and Corrective Bone Surgery, Section VI, Pages 749-755
Book Chapter
Dysostosen (lokalisierte hereditäre skelettale Fehlbildungen)
2006, Kinderorthopädie in der Praxis, 4, 4.6, Pages 684-686