How to Cite this Article: Holman SK, Daniel P, Jenkins ZA, Herron RL, Morgan T, Savarirayan R, Chow CW, Bohring A, Mosel A, Lacombe D, Steiner B, Schmitt-Mechelke T, Schroter B, Raas-Rothschild A, Miñaur SG, Porteous M, Parker M, Quarrell O, Tapon D, Cormier-Daire V, Mansour S, Nash R, Bindoff LA, Fiskerstrand T, Robertson SP. 2011. The male phenotype in osteopathia striata congenita with cranial sclerosis. Am J Med Genet Part A 155:2397–2408.
The male phenotype in osteopathia striata congenita with cranial sclerosis†
Version of Record online: 16 AUG 2011
Copyright © 2011 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 155, Issue 10, pages 2397–2408, October 2011
How to Cite
Holman, S. K., Daniel, P., Jenkins, Z. A., Herron, R. L., Morgan, T., Savarirayan, R., Chow, C.W., Bohring, A., Mosel, A., Lacombe, D., Steiner, B., Schmitt-Mechelke, T., Schroter, B., Raas-Rothschild, A., Miñaur, S. G., Porteous, M., Parker, M., Quarrell, O., Tapon, D., Cormier-Daire, V., Mansour, S., Nash, R., Bindoff, L. A., Fiskerstrand, T. and Robertson, S. P. (2011), The male phenotype in osteopathia striata congenita with cranial sclerosis. Am. J. Med. Genet., 155: 2397–2408. doi: 10.1002/ajmg.a.34178
- Issue online: 20 SEP 2011
- Version of Record online: 16 AUG 2011
- Manuscript Accepted: 8 MAR 2011
- Manuscript Received: 14 DEC 2010
- Curekids New Zealand
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