Browsing by Author Garcia-Ortiz, J.E.

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A familial case of Cantu craniofaciofronto digital syndromeGarcia-Gonzalez, C.L.; Garcia-Cruz, D.; Garcia-Cruz, M.O.; Castaneda-Cisneros, G.; Garcia-Ortiz, J.E.; Orozco-Gutierrez, M.H.; Sanchez-Corona, J.--
A familial case of Cantu craniofaciofronto digital syndromeGarcia-Gonzalez, C.L.; Garcia-Cruz, D.; Garcia-Cruz, M.O.; Castaneda-Cisneros, G.; Garcia-Ortiz, J.E.; Orozco-Gutierrez, M.H.; Sanchez-Corona, J.--
A novel HLA-A allele: A*0257Garcia-Ortiz, J.E.; Cox, S.T.; Sandoval-Ramirez, L.; Little, A.M.; Marsh, S.G.E.; Madrigal, J.A.; Arguello, J.R.--
A novel HLA-A allele: A*0257Garcia-Ortiz, J.E.; Cox, S.T.; Sandoval-Ramirez, L.; Little, A.M.; Marsh, S.G.E.; Madrigal, J.A.; Arguello, J.R.--
Apolipoprotein e genotypes in Mexican patients with Parkinson's diseaseGallegos-Arreola, M.P.; Figuera, L.E.; Ortiz, G.G.; Jimenez-Gil, F.J.; Ramirez-Vega, J.; Ruiz-Sandoval, J.L.; Puebla-Perez, A.M.; Troyo-Sanroman, R.; Garcia-Ortiz, J.E.; Sanchez-Corona, J.; Zuniga-Gonzalez, G.M.--
Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the rozin camptodactyly syndrome [3]Garcia-Ortiz, J.E.; Castaneda-Cisneros, G.; Lopez-Cardona, M.G.; Sanchez-Corona, J.; Patino-Garcia, B.; Garcia-Gonzalez, C.L.; Nazara, Z.; Davalos-Rodriguez, N.; Rodriguez, L.X.; Garcia-Cruz, D.--
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.--
Complete achromatopsia associated with skeletal anomalies: A new autosomal recessive syndromeGarcia-Ortiz, J.E.; Garcia-Cruz, D.; Mendoza-Topete, R.; Quiroz-Mercado, H.; Garcia-Cruz, M.O.; Sanchez-Corona, J.--
Complete achromatopsia associated with skeletal anomalies: A new autosomal recessive syndromeGarcia-Ortiz, J.E.; Garcia-Cruz, D.; Mendoza-Topete, R.; Quiroz-Mercado, H.; Garcia-Cruz, M.O.; Sanchez-Corona, J.--
Familial iridogoniodysgenesis and skeletal anomalies: A probable new autosomal recessive disorderRodriguez-Rojas, L.X.; Garcia-Cruz, D.; Mendoza-Topete, R.; Barba, L.B.; Barrios, M.T.; Patino-Garcia, B.; Lopez-Cardona, M.G.; Nuno-Arana, I.; Garcia-Ortiz, J.E.; Cantu, J.M.--
Familial iridogoniodysgenesis and skeletal anomalies: A probable new autosomal recessive disorderRodriguez-Rojas, L.X.; Garcia-Cruz, D.; Mendoza-Topete, R.; Barba, L.B.; Barrios, M.T.; Patino-Garcia, B.; Lopez-Cardona, M.G.; Nuno-Arana, I.; Garcia-Ortiz, J.E.; Cantu, J.M.--
High-resolution molecular characterization of the HLA class I and class II in the Tarahumara Amerindian populationGarcia-Ortiz, J.E.; Sandoval-Ramirez, L.; Rangel-Villalobos, H.; Maldonado-Torres, H.; Cox, S.; Garcia-Sepulveda, C.A.; Figuera, L.E.; Marsh, S.G.E.; Little, A.M.; Madrigal, J.A.; Moscoso, J.; Arnaiz-Villena, A.; Arguello, J.R.--
Human leukocyte antigen G (HLA-G) as a biomarker in cancer [Antígeno leucocitario humano g (Hla-g) como biomarcador en cáncer]Porras-Dorantes, A.; Garcia-Ortiz, J.E.--
Human leukocyte antigen G (HLA-G) as a biomarker in cancer [Antígeno leucocitario humano g (Hla-g) como biomarcador en cáncer]Porras-Dorantes, A.; Garcia-Ortiz, J.E.--
Microcephaly, distinctive facies, single atrium, postaxial polydactyly, skeletal defects and mental retardation: A new familial faciocardiomelic syndrome?Garcia-Ortiz, J.E.; Garcia-Cruz, D.; Davalos, I.P.; Nazara, Z.; Garcia-Cruz, M.O.; Castaneda, V.; Gutierrez-Mendivil, L.; Sanchez-Corona, J.--
Myhre syndrome: First female caseDavalos, N.O.; Garcia-Ortiz, J.E.; Garcia-Cruz, D.; Feria-Velasco, A.; Sanchez-Corona, J.--
Myhre syndrome: First female caseDavalos, N.O.; Garcia-Ortiz, J.E.; Garcia-Cruz, D.; Feria-Velasco, A.; Sanchez-Corona, J.--
Second female case of Myhre syndromeLopez-Cardona, M.G.; Garcia-Cruz, D.; Garcia-Ortiz, J.E.; Davalos, N.O.; Feria-Velasco, A.; Rodriguez-Rojas, L.X.; Garcia-Cruz, M.O.; Figuera-Villanueva, L.E.; Stephens, A.; Larios-Arceo, F.; Sanchez-Corona, J.--
Second female case of Myhre syndromeLopez-Cardona, M.G.; Garcia-Cruz, D.; Garcia-Ortiz, J.E.; Davalos, N.O.; Feria-Velasco, A.; Rodriguez-Rojas, L.X.; Garcia-Cruz, M.O.; Figuera-Villanueva, L.E.; Stephens, A.; Larios-Arceo, F.; Sanchez-Corona, J.--
SED-brachydactyly and distinctive speech: Report of two new casesGarcia-Cruz, D.; Zafra De La Rosa, G.F.; Sanchez-Corona, J.; Nazara, Z.; Lopez-Cardona, M.G.; Garcia-Ortiz, J.E.; Corona-Rivera, J.R.; Cantu, J.M.--