A missense mutation, p.V132G, in the X-linked spermine synthase gene (SMS) causes Snyder-Robinson syndrome by Becerra-Solano, L.E., Butler, J., Castañeda-Cisneros, G., McCloskey, D.E., Wang, X., Pegg, A.E., Schwartz, C.E., Sánchez-Corona, J., García-Ortiz, J.E.

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Consenso mexicano sobre el diagnóstico de la deficiencia de lipasa ácida lisosomal by Vázquez-Frias, R, García-Ortiz, J.E, Valencia-Mayoral, P.F, Castro-Narro, G.E, Medina-Bravo, P.G, Santillán-Hernández, Y, Flores-Calderón, J, Mehta, R, Arellano-Valdés, C.A, Carbajal-Rodríguez, L, Navarrete-Martínez, J.I, Urbán-Reyes, M.L, Valadez-Reyes, M.T, Zárate-Mondragón, F, Consuelo- Sánchez, A

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Mexican consensus on lysosomal acid lipase deficiency diagnosis by Vázquez-Frias, R., García-Ortiz, J.E., Valencia-Mayoral, P.F., Castro-Narro, G.E., Medina-Bravo, P.G., Santillán-Hernández, Y., Flores-Calderón, J., Mehta, R., Arellano-Valdés, C.A., Carbajal-Rodríguez, L., Navarrete-Martínez, J.I., Urbán-Reyes, M.L., Valadez-Reyes, M.T., Zárate-Mondragón, F., Consuelo-Sánchez, A.

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Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the Rozin camptodactyly syndrome by García-Ortiz, J.E., Castañeda-Cisneros, G., López-Cardona, M.G., Sánchez-Corona, J., Patiño-García, B., García-González, C.L., Nazará, Z., Dávalos-Rodríguez, N., Rodríguez, L.X., García-Cruz, D.

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Molecular thrombophilic profile in Mexican patients with idiopathic recurrent pregnancy loss by López-Jiménez, J J, Porras-Dorantes, Á, Juárez-Vázquez, C I, García-Ortiz, J E, Fuentes-Chávez, C A, Lara-Navarro, I J, Jaloma-Cruz, A R

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Metaphyseal chondrodysplasia, upper limb mesomelia and normal height (mesomelic dysplasia camera type): Second report in a Mexican patient by Becerra‐Solano, L.E., Castañeda‐Cisneros, G., Bañuelos‐Acosta, R., Sánchez‐Corona, J., García‐Ortiz, J.E.

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Apolipoprotein E genotypes in Mexican patients with Parkinson's disease by Gallegos-Arreola, M P, Figuera, L E, Ortiz, G G, Jiménez-Gil, F J, Ramírez-Vega, J, Ruíz-Sandoval, J L, Puebla-Pérez, A M, Troyo-Sanroman, R, García-Ortiz, J E, Sanchez-Corona, J, Zúñiga-González, G M

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Apolipoprotein E genotypes in Mexican patients with Parkinson's disease by Gallegos-Arreola, M P, Figuera, L E, Ortiz, G G, Jiménez-Gil, F J, Ramírez-Vega, J, Ruíz-Sandoval, J L, Puebla-Pérez, A M, Troyo-Sanroman, R, García-Ortiz, J E, Sanchez-Corona, J, Zúñiga-González, G M

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A novel HLA-A allele: A0257 by García-Ortiz, J.E., Cox, S.T., Sandoval-Ramirez, L., Little, A.M., Marsh, S.G.E., Madrigal, J.A., Argüello, J.R.

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p63 gene analysis in Mexican patients with syndromic and non-syndromic ectrodactyly by Berdón-Zapata, V, Granillo-Álvarez, M, Valdés-Flores, M, Garcı́a-Ortiz, J.E, Kofman-Alfaro, S, Zenteno, J.C

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Metaphyseal chondrodysplasia, upper limb mesomelia and normal height (mesomelic dysplasia camera type): Second report in a Mexican patient by Becerra-Solano, L.E., Castañeda-Cisneros, G., Bañuelos-Acosta, R., Sánchez-Corona, J., García-Ortiz, J.E.

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