M. Roifman Et Al. , "De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype," CLINICAL GENETICS , vol.87, no.1, pp.34-41, 2015
Roifman, M. Et Al. 2015. De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. CLINICAL GENETICS , vol.87, no.1 , 34-41.
Roifman, M., Marcelis, C. L. M., Paton, T., Marshall, C., Silver, R., Lohr, J. L., ... Yntema, H. G.(2015). De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. CLINICAL GENETICS , vol.87, no.1, 34-41.
Roifman, M. Et Al. "De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype," CLINICAL GENETICS , vol.87, no.1, 34-41, 2015
Roifman, M. Et Al. "De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype." CLINICAL GENETICS , vol.87, no.1, pp.34-41, 2015
Roifman, M. Et Al. (2015) . "De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype." CLINICAL GENETICS , vol.87, no.1, pp.34-41.
@article{article, author={M. Roifman Et Al. }, title={De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype}, journal={CLINICAL GENETICS}, year=2015, pages={34-41} }