J. Halbritter Et Al. , "Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans," AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.5, pp.915-925, 2013
Halbritter, J. Et Al. 2013. Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans. AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.5 , 915-925.
Halbritter, J., Bizet, A. A., Schmidts, M., Porath, J. D., Braun, D. A., Gee, H. Y., ... McInerney-Leo, A. M.(2013). Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans. AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.5, 915-925.
Halbritter, Jan Et Al. "Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans," AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.5, 915-925, 2013
Halbritter, Jan Et Al. "Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans." AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.5, pp.915-925, 2013
Halbritter, J. Et Al. (2013) . "Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans." AMERICAN JOURNAL OF HUMAN GENETICS , vol.93, no.5, pp.915-925.
@article{article, author={Jan Halbritter Et Al. }, title={Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans}, journal={AMERICAN JOURNAL OF HUMAN GENETICS}, year=2013, pages={915-925} }