Browsing by Author Mantilla-Capacho, J.M.

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Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 geneMantilla-Capacho, J.M.; Arnaud, L.; Diaz-Rodriguez, M.; Barros-Nunez, P.--
Apert syndrome with preaxial polydactyly showing the typical mutation Ser252Trp in the FGFR2 geneMantilla-Capacho, J.M.; Arnaud, L.; Diaz-Rodriguez, M.; Barros-Nunez, P.--
Clinical variability of haemophilia A and B in Mexican families by factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T/A1298CLopez-Jimenez, J.J.; Beltran-Miranda, C.P.; Mantilla-Capacho, J.M.; Esparza-Flores, M.A.; Lopez Gonzalez, L.C.; Jaloma-Cruz, A.R.--
Clinical variability of haemophilia A and B in Mexican families by factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T/A1298CLopez-Jimenez, J.J.; Beltran-Miranda, C.P.; Mantilla-Capacho, J.M.; Esparza-Flores, M.A.; Lopez Gonzalez, L.C.; Jaloma-Cruz, A.R.--
First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patientBecerra-Solano, L.E.; Arnaud-Lopez, L.; Diaz-Rodriguez, M.; Mantilla-Capacho, J.M.; Nastasi-Catanese, J.A.; Ortiz-Aranda, M.; Vasquez, A.I.; Figuera, L.E.--
First case reported of Turner syndrome and trisomy 14 chromosomal mosaicism in a patientBecerra-Solano, L.E.; Arnaud-Lopez, L.; Diaz-Rodriguez, M.; Mantilla-Capacho, J.M.; Nastasi-Catanese, J.A.; Ortiz-Aranda, M.; Vasquez, A.I.; Figuera, L.E.--
Frequency of intron 1 and 22 inversions of factor VIII gene in Mexican patients with severe hemophilia AMantilla-Capacho, J.M.; Beltran-Miranda, C.P.; Luna-Zaizar, H.; Aguilar-Lopez, L.; Esparza-Flores, M.A.; Lopez-Guido, B.; Troyo-Sanroman, R.; Jaloma-Cruz, A.R.--
Gaussians on the circle and quantum phaseMantilla-Capacho, J.M.; Beltran-Miranda, C.P.; Luna-Zaizar, H.; Aguilar-Lopez, L.; Esparza-Flores, M.A.; Lopez-Guido, B.; Troyo-Sanroman, R.; Jaloma-Cruz, A.R.--
Phenotypic variability in a family with haemophilia B and prothrombin G20210ABeltran-Miranda, C.P.; Luna-Zaizar, H.; Lopez-Jimenez, J.J.; Mantilla-Capacho, J.M.; Laffan, M.; Jaloma-Cruz, A.R.--
Phenotypic variability in a family with haemophilia B and prothrombin G20210ABeltran-Miranda, C.P.; Luna-Zaizar, H.; Lopez-Jimenez, J.J.; Mantilla-Capacho, J.M.; Laffan, M.; Jaloma-Cruz, A.R.--