Child, Preschool
M. F. Mattos, Uback, L., Biselli-Chicote, P. M., Biselli, J. M., Goloni-Bertollo, E. M., and Pavarino, E. C.,
“Polymorphisms of interleukin 6 in Down syndrome individuals: a case-control study.”,
Genet Mol Res, vol. 16, no. 3, 2017.
A. F. Nascimento, Oliveira, J. S., Junior, J. C. Silva, and Barbosa, A. A. L.,
“Haplotypes and polymorphism in the CCR5 gene in sickle cell disease.”,
Genet Mol Res, vol. 16, no. 2, 2017.
R. E. Jiménez-Arredondo, Brambila-Tapia, A. J. L., Mercado-Silva, F. M., Magaña-Torres, M. T., and Figuera, L. E.,
“Determination of SCN1A genetic variants in Mexican patients with refractory epilepsy and Dravet syndrome.”,
Genet Mol Res, vol. 16, no. 2, 2017.
G. Y. Lin, Du, X. L., Shan, J. J., Zhang, Y. N., Zhang, Y. Q., and Wang, Q. H.,
“MNS, Duffy, and Kell blood groups among the Uygur population of Xinjiang, China.”,
Genet Mol Res, vol. 16, no. 1, 2017.
P. H. S. Klinger, Andrade, A. F., Delsin, L. E. A., Queiroz, R. G. P., Scrideli, C. A., Tone, L. G., and Valera, E. T.,
“Inhibition of SHH pathway mechanisms by arsenic trioxide in pediatric medulloblastomas: a comprehensive literature review.”,
Genet Mol Res, vol. 16, no. 1, 2017.
