Author:
Abo-Dalo Benjamin,Roes Melanie,Canún Sonia,Delatycki Martin,Gillessen-Kaesbach Gabriele,Hrytsiuk Ihor,Jung Christine,Kerr Bronwyn,Mowat David,Seemanova Eva,Steiner Carlos E.,Stewart Helen,Thierry Patrick,van Buggenhout Griet,White Sue,Zenker Martin,Kutsche Kerstin
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health
Reference16 articles.
1. Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann–Laband syndrome;Abo-Dalo;Am J Med Genet A,2007
2. Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia;Bergmann;Am J Hum Genet,2006
3. The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia;Blaydon;Nat Genet,2006
4. Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: a new distinct entity;Canun;Am J Med Genet,2003
5. Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition?;Göhlich-Ratmann;Am J Med Genet,2000
Cited by
10 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