No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome
- PMID: 18541964
- DOI: 10.1097/MCD.0b013e3282f2514c
No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome
References
-
- Abo-Dalo B, Kim HG, Roes M, Stefanova M, Higgins A, Shen Y, et al. 2007. Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann–Laband syndrome. Am J Med Genet A 143:2668–2674.
-
- Bergmann C, Senderek J, Anhuf D, Thiel CT, Ekici AB, Poblete-Gutierrez P, et al. 2006. Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia. Am J Hum Genet 79:1105–1109.
-
- Blaydon DC, Ishii Y, O'Toole EA, Unsworth HC, The MT, Ruschendorf F, et al. 2006. The gene encoding R-spondin 4 (RSPO4), a secreted protein implicated in Wnt signaling, is mutated in inherited anonychia. Nat Genet 38:1245–1247.
-
- Canun S, Guevara-Sangines EG, Elvira-Morales A, Sierra-Romero Mdel C, Rodriguez-Asbun H 2003. Hypertrichosis terminalis, gingival hyperplasia, and a characteristic face: a new distinct entity. Am J Med Genet 116:278–283.
-
- Göhlich-Ratmann G, Lackner A, Schaper J, Voit T, Gillessen-Kaesbach G 2000. Syndrome of gingival hypertrophy, hirsutism, mental retardation and brachymetacarpia in two sisters: specific entity or variant of a described condition? Am J Med Genet 95:241–246.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases
