Author:
Gilissen Christian,Arts Heleen H.,Hoischen Alexander,Spruijt Liesbeth,Mans Dorus A.,Arts Peer,van Lier Bart,Steehouwer Marloes,van Reeuwijk Jeroen,Kant Sarina G.,Roepman Ronald,Knoers Nine V.A.M.,Veltman Joris A.,Brunner Han G.
Subject
Genetics (clinical),Genetics
Reference24 articles.
1. New syndrome of skeletal, dental and hair anomalies;Sensenbrenner;Birth Defects Orig. Artic. Ser.,1975
2. A heritable syndrome of craniosynostosis, short thin hair, dental abnormalities, and short limbs: Cranioectodermal dysplasia;Levin;J. Pediatr.,1977
3. Expanded phenotype of cranioectodermal dysplasia (Sensenbrenner syndrome);Amar;Am. J. Med. Genet.,1997
4. Making sense of cilia in disease: The human ciliopathies;Baker;Am. J. Med. Genet. C Semin. Med. Genet.,2009
5. Cranioectodermal dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene;Walczak-Sztulpa;Am. J. Hum. Genet.,2010
Cited by
243 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