Schmidts, M. Et Al. 2013. 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 , vol.50, no.5 , 309-323.

Schmidts, M., Arts, H. H., Bongers, E. M. H. F., Yap, Z., Oud, M. M., Antony, D., ... Duijkers, L.(2013). 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 , vol.50, no.5, 309-323.

Schmidts, Miriam Et Al. "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 , vol.50, no.5, 309-323, 2013

Schmidts, Miriam Et Al. "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 , vol.50, no.5, pp.309-323, 2013

Schmidts, M. Et Al. (2013) . "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 , vol.50, no.5, pp.309-323.

@article{article, author={Miriam Schmidts Et Al. }, title={Exome sequencing identifies DYNC2H1 mutations as a common cause of asphyxiating thoracic dystrophy (Jeune syndrome) without major polydactyly, renal or retinal involvement}, journal={JOURNAL OF MEDICAL GENETICS}, year=2013, pages={309-323} }