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A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype
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P. A. Terhal Et Al. , "A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.3, pp.461-475, 2015

Terhal, P. A. Et Al. 2015. A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.3 , 461-475.

Terhal, P. A., Nievelstein, R. J. A. J., Verver, E. J. J., Topsakal, V., van Dommelen, P., Hoornaert, K., ... Le Merrer, M.(2015). A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype. AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.3, 461-475.

Terhal, Paulien Et Al. "A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype," AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.3, 461-475, 2015

Terhal, Paulien A. Et Al. "A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.3, pp.461-475, 2015

Terhal, P. A. Et Al. (2015) . "A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype." AMERICAN JOURNAL OF MEDICAL GENETICS PART A , vol.167, no.3, pp.461-475.

@article{article, author={Paulien A. Terhal Et Al. }, title={A Study of the Clinical and Radiological Features in a Cohort of 93 Patients with a COL2A1 Mutation Causing Spondyloepiphyseal Dysplasia Congenita or a Related Phenotype}, journal={AMERICAN JOURNAL OF MEDICAL GENETICS PART A}, year=2015, pages={461-475} }