Browsing by Author Rojas-Martinez, A.

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A de novo sSMC(22) characterized by high-resolution arrays in a girl with cat-eye syndrome without colobomaCordova-Fletes, C.; Dominguez, M.G.; Vazquez-Cardenas, A.; Figuera, L.E.; Neira, V.A.; Rojas-Martinez, A.; Ortiz-Lopez, R.--
A de novo sSMC(22) characterized by high-resolution arrays in a girl with cat-eye syndrome without colobomaCordova-Fletes, C.; Dominguez, M.G.; Vazquez-Cardenas, A.; Figuera, L.E.; Neira, V.A.; Rojas-Martinez, A.; Ortiz-Lopez, R.--
Ancestry informative markers and admixture proportions in northeastern MexicoMartinez-Fierro, M.L.; Beuten, J.; Leach, R.J.; Parra, E.J.; Cruz-Lopez, M.; Rangel-Villalobos, H.; Riego-Ruiz, L.R.; Ortiz-Lopez, R.; Martinez-Rodriguez, H.G.; Rojas-Martinez, A.--
Ancestry informative markers and admixture proportions in northeastern MexicoMartinez-Fierro, M.L.; Beuten, J.; Leach, R.J.; Parra, E.J.; Cruz-Lopez, M.; Rangel-Villalobos, H.; Riego-Ruiz, L.R.; Ortiz-Lopez, R.; Martinez-Rodriguez, H.G.; Rojas-Martinez, A.--
De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome featuresNeira, V.A.; Romero-Espinoza, P.; Rojas-Martinez, A.; Ortiz-Lopez, R.; Cordova-Fletes, C.; Plaja, A.; Barros-Nunez, P.--
De novo MECP2 disomy in a Mexican male carrying a supernumerary marker chromosome and no typical Lubs syndrome featuresNeira, V.A.; Romero-Espinoza, P.; Rojas-Martinez, A.; Ortiz-Lopez, R.; Cordova-Fletes, C.; Plaja, A.; Barros-Nunez, P.--
Poland-Moebius syndrome in a boy and Poland Syndrome in his motherRojas-Martinez, A.; Garcia-Cruz, D.; Rodriguez Garcia, A.; Sanchez-Corona, J.; Rivas, F.--
Poland-Moebius syndrome in a boy and Poland Syndrome in his motherRojas-Martinez, A.; Garcia-Cruz, D.; Rodriguez Garcia, A.; Sanchez-Corona, J.; Rivas, F.--