Craniosynostoses —— Molecular Genetics, Principles of Diagnosis, and Treatment

----- 颅缝早闭:分子遗传学、诊断原理及治疗

ISBN: 9783805595940 出版年：2011 页码：259 S.Karger

Editorial: Schmid, M. Preface: Muenke, M. Kress, W. Collmann, H. Solomon, B.D. Foreword: Cohen Jr., M.M. Craniosynostosis: A Historical Overview: Solomon, B.D. Collmann, H. Kress, W. Muenke, M. Discovery of MSX2 Mutation in Craniosynostosis: A Retrospective View: Muller, U. Regulation of Calvarial Bone Growth by Molecules Involved in the Craniosynostoses: Benson, M.D. Opperman, L.A. Signal Transduction Pathways and Their Impairment in Syndromic Craniosynostosis: Connerney, J.J. Spicer, D.B. The Molecular Bases for FGF Receptor Activation in Craniosynostosis and Dwarfism Syndromes: Beenken, A. Mohammadi, M. Recurrent Germline Mutations in the FGFR2/3 Genes, High Mutation Frequency, Paternal Skewing and Age-Dependence: Arnheim, N. Calabrese, P. Apert, Crouzon, and Pfeiffer Syndromes: Cohen Jr., M.M. Muenke Syndrome: Solomon, B.D. Muenke, M. Saethre-Chotzen Syndrome: Clinical and Molecular Genetic Aspects: Kress, W. Collmann, H. Craniofrontonasal Syndrome: Molecular Genetics, EFNB1 Mutations and the Concept of Cellular Interference: Wieland, I. Uncommon Craniosynostosis Syndromes: A Review of Thirteen Conditions: Raam, M.S. Muenke, M. Metopic Craniosynostosis Syndrome Due to Mutations in GLI3: McDonald-McGinn, D.M. Feret, H. Nah, H.-D. Zackai, E.H. Craniosynostosis and Chromosomal Alterations: Passos-Bueno, M.R. Fanganiello, R.D. Jehee, F.S. Nonsyndromic Craniosynostoses: Collmann, H. Solomon, B.D. Schweitzer, T. Kress, W. Muenke, M. Molecular Genetic Testing of Patients with Craniosynostosis: Hehr, U. Prenatal Sonographic Diagnosis of Craniosynostosis: Schramm, T. Clinical Approach to Craniosynostosis: Gripp, K.W. Imaging Studies and Neurosurgical Treatment: Collmann, H. Schweitzer, T. Bohm, H. Maxillofacial Examination and Treatment: Bohm, H. Schweitzer, T. Kubler, A. Author and Subject Index.