A. Willaert Et Al. , "Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation," JOURNAL OF MEDICAL GENETICS , vol.46, no.4, pp.233-241, 2009
Willaert, A. Et Al. 2009. Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation. JOURNAL OF MEDICAL GENETICS , vol.46, no.4 , 233-241.
Willaert, A., Malfait, F., Symoens, S., Gevaert, K., Kayserili, H., Megarbane, A., ... Mortier, G.(2009). Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation. JOURNAL OF MEDICAL GENETICS , vol.46, no.4, 233-241.
Willaert, A. Et Al. "Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation," JOURNAL OF MEDICAL GENETICS , vol.46, no.4, 233-241, 2009
Willaert, A. Et Al. "Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation." JOURNAL OF MEDICAL GENETICS , vol.46, no.4, pp.233-241, 2009
Willaert, A. Et Al. (2009) . "Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation." JOURNAL OF MEDICAL GENETICS , vol.46, no.4, pp.233-241.
@article{article, author={A. Willaert Et Al. }, title={Recessive osteogenesis imperfecta caused by LEPRE1 mutations: clinical documentation and identification of the splice form responsible for prolyl 3-hydroxylation}, journal={JOURNAL OF MEDICAL GENETICS}, year=2009, pages={233-241} }