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. 2008 Jul;17(3):181-185.
doi: 10.1097/MCD.0b013e3282f2514c.

No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome

Affiliations

No mutation in genes of the WNT signaling pathway in patients with Zimmermann-Laband syndrome

Benjamin Abo-Dalo et al. Clin Dysmorphol. 2008 Jul.
No abstract available

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References

    1. 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.
    1. 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.
    1. 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.
    1. 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.
    1. 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.

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