Browsing by Author Orozco-Castellanos, R.

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Association of the FTO gene SNP rs17817449 with body fat distribution in Mexican womenZermeno-Rivera, J.J.; Astocondor-Perez, J.P.; Valle, Y.; Padilla-Gutierrez, J.R.; Orozco-Castellanos, R.; Figuera, L.E.; Gutierrez-Amavizca, B.E.--
Association of the FTO gene SNP rs17817449 with body fat distribution in Mexican womenZermeno-Rivera, J.J.; Astocondor-Perez, J.P.; Valle, Y.; Padilla-Gutierrez, J.R.; Orozco-Castellanos, R.; Figuera, L.E.; Gutierrez-Amavizca, B.E.--
Contribution of GSTM1, GSTT1, and MTHFR polymorphisms to end-stage renal disease of unknown etiology in MexicansGutierrez-Amavizca, B.E.; Orozco-Castellanos, R.; Ortiz-Orozco, R.; Padilla-Gutierrez, J.; Valle, Y.; Gutierrez-Gutierrez, N.; Garcia-Garcia, G.; Gallegos-Arreola, M.; Figuera, L.E.--
Contribution of GSTM1, GSTT1, and MTHFR polymorphisms to end-stage renal disease of unknown etiology in MexicansGutierrez-Amavizca, B.E.; Orozco-Castellanos, R.; Ortiz-Orozco, R.; Padilla-Gutierrez, J.; Valle, Y.; Gutierrez-Gutierrez, N.; Garcia-Garcia, G.; Gallegos-Arreola, M.; Figuera, L.E.--
[Current genetic issues and phenotypic variants in Kallmann syndrome]. [Síndrome de Kallmann. Aspectos genéticos y variantes fenotípicas.]Gutierrez-Amavizca, B.E.; Figuera, L.E.; Orozco-Castellanos, R.--
[Current genetic issues and phenotypic variants in Kallmann syndrome]. [Síndrome de Kallmann. Aspectos genéticos y variantes fenotópicas.]Gutierrez-Amavizca, B.E.; Figuera, L.E.; Orozco-Castellanos, R.--
Labeling of HeLa cells using ZrO<inf>2</inf>:Yb3+-Er3+ nanoparticles with upconversion emissionGutierrez-Amavizca, B.E.; Orozco-Castellanos, R.; Padilla-Gutierrez, J.R.; Valle, Y.; Figuera, L.E.--
Neuhauser syndrome: A rare association of megalocornea and mental retardation. Review of the literature and further phenotype delineationGutierrez-Amavizca, B.E.; Juarez-Vazquez, C.I.; Orozco-Castellanos, R.; Arnaud, L.; Macias-Gomez, N.M.; Barros-Nunez, P.--
Neuhauser syndrome: A rare association of megalocornea and mental retardation. Review of the literature and further phenotype delineationGutierrez-Amavizca, B.E.; Juarez-Vazquez, C.I.; Orozco-Castellanos, R.; Arnaud, L.; Macias-Gomez, N.M.; Barros-Nunez, P.--
Pedigree analysis of Mexican families with Fabry disease as a powerful tool for identification of heterozygous femalesGutierrez-Amavizca, B.E.; Orozco-Castellanos, R.; Padilla-Gutierrez, J.R.; Valle, Y.; Figuera, L.E.--