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Keywords: Phalanx formation
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Journal Articles

The mutation ROR2 W749X , linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome

Regina Raz, Sigmar Stricker, Elizabetta Gazzerro, Julie L. Clor, Florian Witte, Harakiran Nistala, Stefanie Zabski, Renata C. Pereira, Lisa Stadmeyer, Xiangmin Wang, Lori Gowen, Mark W. Sleeman, George D. Yancopoulos, Ernesto Canalis, Stefan Mundlos, David M. Valenzuela, Aris N. Economides
Journal: Development
Development (2008) 135 (9): 1713–1723.
https://doi.org/10.1242/dev.015149
Published: 1 May 2008
... model for RRS, provide insight into the mechanism of joint specification, and uncover novel roles of Ror2 in the mouse. 26 2 2008 © 2008. 2008 ROR2 receptor Brachydactyly B Phalanx formation Knock-in mouse Recessive Robinow syndrome (RRS, MIM 268310) and autosomal...
View article titled, The mutation ROR2 W749X , linked to human BDB, is a recessive mutation in the mouse, causing brachydactyly, mediating patterning of joints and modeling recessive Robinow syndrome
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Includes: Supplementary data