Browsing by Author Dominguez, M.G.

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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.--
A familial rearrangement(3;5;9) with paternal and maternal transmission leading to a duplication 3p/ deletion 5p infantRivera, H.; Dominguez, M.G.--
A familial rearrangement(3;5;9) with paternal and maternal transmission leading to a duplication 3p/ deletion 5p infantRivera, H.; Dominguez, M.G.--
Callosotomy in a girl with refractory epilepsy and Smith-Magenis syndromeSalinas-Torres, V.M.; Dominguez, M.G.; Ornelas-Arana, M.L.; Rivera, H.--
Callosotomy in a girl with refractory epilepsy and Smith-Magenis syndromeSalinas-Torres, V.M.; Dominguez, M.G.; Ornelas-Arana, M.L.; Rivera, H.--
CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X-linked infantile spasm syndromeCordova-Fletes, C.; Rademacher, N.; Muller, I.; Mundo-Ayala, J.N.; Morales-Jeanhs, E.A.; García-Ortiz, J.E.; Leon-Gil, A.; Rivera, H.; Dominguez, M.G.; Kalscheuer, V.M.--
CDKL5 truncation due to a t(X;2)(p22.1;p25.3) in a girl with X-linked infantile spasm syndromeCordova-Fletes, C.; Rademacher, N.; Muller, I.; Mundo-Ayala, J.N.; Morales-Jeanhs, E.A.; Garcia-Ortiz, J.E.; Leon-Gil, A.; Rivera, H.; Dominguez, M.G.; Kalscheuer, V.M.--
Centromeric association of a microchromosome y in two male patientsDominguez, M.G.; Vasquez, A.I.; Troyo, R.; Ortiz-Aranda, M.; Padilla, J.R.; Hernandez-Zaragoza, G.; Rivas, F.; Rivera, H.--
Centromeric association of a microchromosome y in two male patientsDominguez, M.G.; Vasquez, A.I.; Troyo, R.; Ortiz-Aranda, M.; Padilla, J.R.; Hernandez-Zaragoza, G.; Rivas, F.; Rivera, H.--
Constitutional duplication 11q23 de novo involving the MLL genePartida-Perez, M.; Dominguez, M.G.; Sanchez-Corona, J.; Castaneda-Cisneros, G.; Garcia-Gonzalez, C.L.; Lopez-Cardona, M.G.; Rivera, H.--
Constitutional duplication 11q23 de novo involving the MLL genePartida-Perez, M.; Dominguez, M.G.; Sanchez-Corona, J.; Castaneda-Cisneros, G.; Garcia-Gonzalez, C.L.; Lopez-Cardona, M.G.; Rivera, H.--
CYP1A1 *2B and *4 polymorphisms are associated with lung cancer susceptibility in Mexican patientsRivera, H.; Dominguez, M.G.; Vasquez-Velasquez, A.I.; Lurie, I.W.--
De novo dup p/del q or dup q/del p rearranged chromosomes: Review of 104 cases of a distinct chromosomal mutationRivera, H.; Dominguez, M.G.; Vasquez-Velasquez, A.I.; Lurie, I.W.--
De novo inv(17)(p11.2q21.3) in an intellectually disabled girl: Appraisal of 21 inv(17) constitutional instancesPartida-Perez, M.; Dominguez, M.G.; Neira, V.A.; Figuera, L.E.; Rivera, H.--
De novo inv(17)(p11.2q21.3) in an intellectually disabled girl: Appraisal of 21 inv(17) constitutional instancesPartida-Perez, M.; Dominguez, M.G.; Neira, V.A.; Figuera, L.E.; Rivera, H.--
Follow-up of an intelligent odd-mannered teenager with del(3)(p26). Remarks on authorship and ethical commitmentRivera, H.; Dominguez, M.G.; Matute, E.--
Follow-up of an intelligent odd-mannered teenager with del(3)(p26). Remarks on authorship and ethical commitmentRivera, H.; Dominguez, M.G.; Matute, E.--
How exhaustive are reviews in research review articles? [4]Rivera, H.; Dominguez, M.G.--
How exhaustive are reviews in research review articles? [4]Rivera, H.; Dominguez, M.G.--