APA
Schmidts M., Arts H. H., Bongers E. M. H. F., Yap Z., Oud M. M., Antony D., Duijkers L., Emes R. D., Stalker J., Yntema J. L., Plagnol V., Hoischen A., Gilissen C., Forsythe E., Lausch E., Veltman J. A., Roeleveld N., Superti-Furga A., Kutkowska-Kazmierczak A., Kamsteeg E., Elçioğlu N., van Maarle M. C., Graul-Neumann L. M., Devriendt K., Smithson S. F., Wellesley D., Verbeek N. E., Hennekam R. C. M., Kayserili H., Scambler P. J., Beales P. L., Knoers N. V., Roepman R. & Mitchison H. M. (20131018). Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. : Journal of medical genetics.
Chicago
Schmidts Miriam, Arts Heleen H, Bongers Ernie M H F, Yap Zhimin, Oud Machteld M, Antony Dinu, Duijkers Lonneke, Emes Richard D, Stalker Jim, Yntema Jan-Bart L, Plagnol Vincent, Hoischen Alexander, Gilissen Christian, Forsythe Elisabeth, Lausch Ekkehart, Veltman Joris A, Roeleveld Nel, Superti-Furga Andrea, Kutkowska-Kazmierczak Anna, Kamsteeg Erik-Jan, Elçioğlu Nursel, van Maarle Merel C, Graul-Neumann Luitgard M, Devriendt Koenraad, Smithson Sarah F, Wellesley Diana, Verbeek Nienke E, Hennekam Raoul C M, Kayserili Hulya, Scambler Peter J, Beales Philip L, Knoers Nine Vam, Roepman Ronald and Mitchison Hannah M. 20131018. Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. : Journal of medical genetics.
Harvard
Schmidts M., Arts H. H., Bongers E. M. H. F., Yap Z., Oud M. M., Antony D., Duijkers L., Emes R. D., Stalker J., Yntema J. L., Plagnol V., Hoischen A., Gilissen C., Forsythe E., Lausch E., Veltman J. A., Roeleveld N., Superti-Furga A., Kutkowska-Kazmierczak A., Kamsteeg E., Elçioğlu N., van Maarle M. C., Graul-Neumann L. M., Devriendt K., Smithson S. F., Wellesley D., Verbeek N. E., Hennekam R. C. M., Kayserili H., Scambler P. J., Beales P. L., Knoers N. V., Roepman R. and Mitchison H. M. (20131018). Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. : Journal of medical genetics.
MLA
Schmidts Miriam, Arts Heleen H, Bongers Ernie M H F, Yap Zhimin, Oud Machteld M, Antony Dinu, Duijkers Lonneke, Emes Richard D, Stalker Jim, Yntema Jan-Bart L, Plagnol Vincent, Hoischen Alexander, Gilissen Christian, Forsythe Elisabeth, Lausch Ekkehart, Veltman Joris A, Roeleveld Nel, Superti-Furga Andrea, Kutkowska-Kazmierczak Anna, Kamsteeg Erik-Jan, Elçioğlu Nursel, van Maarle Merel C, Graul-Neumann Luitgard M, Devriendt Koenraad, Smithson Sarah F, Wellesley Diana, Verbeek Nienke E, Hennekam Raoul C M, Kayserili Hulya, Scambler Peter J, Beales Philip L, Knoers Nine Vam, Roepman Ronald and Mitchison Hannah M. Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement. : Journal of medical genetics. 20131018.