Standard variant venous dysplasia of the cerebellum in a patient suffering from Muenke's syndrome and tinnitus
Author:
Publisher
Elsevier BV
Subject
General Medicine,Otorhinolaryngology,Surgery
Reference7 articles.
1. FGFR2 mutations in Peiffer Syndrome;Lajeunie;Nat. Genet.,1995
2. Fibroblast growth factor receptor mutations in human skeletal disorders;Muenke;Trends Genet.,1995
3. Syndromes with craniosynostosis;Cohen,1986
4. Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes;Bellus;Nat. Genet.,1996
5. Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to pro250arg mutation in FGFR 3 gene;Graham;Am. J. Med. Genet.,1998
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Expansion of the variable expression of Muenke syndrome: Hydrocephalus without craniosynostosis;American Journal of Medical Genetics Part A;2016-08-29
2. Muenke syndrome (FGFR3-related craniosynostosis): Expansion of the phenotype and review of the literature;American Journal of Medical Genetics Part A;2007
3. Tinnitus and Cerebellar Developmental Venous Anomaly;Archives of Otolaryngology–Head & Neck Surgery;2006-05-01
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