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	1.	Mutations in DVL1 cause an osteosclerotic form of Robinow syndrome. [electronic resource] by Bunn, Kieran J Daniel, Phil Rösken, Heleen S O'Neill, Adam C Cameron-Christie, Sophia R Morgan, Tim Brunner, Han G Lai, Angeline Kunst, Henricus P M Markie, David M Robertson, Stephen P Producer: 20150529 In: American journal of human genetics vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The male phenotype in osteopathia striata congenita with cranial sclerosis. [electronic resource] by Holman, Sarah K Daniel, Phil Jenkins, Zandra A Herron, Rachel L Morgan, Tim Savarirayan, Ravi Chow, C W Bohring, Axel Mosel, Annette Lacombe, Didier Steiner, Bernhard Schmitt-Mechelke, Thomas Schroter, Barbara Raas-Rothschild, Annick Miñaur, Sixto Garcia Porteous, Mary Parker, Michael Quarrell, Oliver Tapon, Dagmar Cormier-Daire, Valérie Mansour, Sahar Nash, Ruth Bindoff, Laurence A Fiskerstrand, Torunn Robertson, Stephen P Producer: 20120118 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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