Browsing by Author Garcia-Cruz, D.

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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.--
Cantu syndrome and lymphoedemaGarcia-Cruz, D.; Mampel, A.; Echeverria, M.I.; Vargas, A.L.; Castaneda-Cisneros, G.; Davalos-Rodriguez, N.; Patino-Garcia, B.; Garcia-Cruz, M.O.; Castaneda, V.; Cardona, E.G.; Marin-Solis, B.; Cantu, J.M.; Nunez-Reveles, N.; Moran-Moguel, C.; Thavanati, P.K.R.; Ramirez-Garcia, S.; Sanchez-Corona, J.--
Chromosome Instability Induced in Vitro with Mitomycin C in Five Seckel Syndrome PatientsBobabilla-Morales, L.; Corona-Rivera, A.; Corona-Rivera, J.R.; Buenrostro, C.; Garcia-Cobian, T.A.; Corona-Rivera, E.; Cantu-Garza, J.M.; Garcia-Cruz, D.--
Chromosome Instability Induced in Vitro with Mitomycin C in Five Seckel Syndrome PatientsBobabilla-Morales, L.; Corona-Rivera, A.; Corona-Rivera, J.R.; Buenrostro, C.; Garcia-Cobian, T.A.; Corona-Rivera, E.; Cantu-Garza, J.M.; Garcia-Cruz, D.--
Clinical, morphological and biochemical features in the familial articular hypermobility syndrome (FAHS): A family studyGarcia-Cruz, D.; Cano-Colin, S.; Sanchez-Corona, J.; Gallegos, M.P.; Chimal-Monroy, J.; Diaz-de-Leon, L.--
Clinical, morphological and biochemical features in the familial articular hypermobility syndrome (FAHS): A family studyGarcia-Cruz, D.; Cano-Colin, S.; Sanchez-Corona, J.; Gallegos, M.P.; Chimal-Monroy, J.; Diaz-de-Leon, L.--
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.--
Confirmation of tyrosine 698 in beta subunit of cGMP phosphodiesterase in patients with retinitis pigmentosa and population of the west of MexicoNunez-Gutierrez, I.C.; Garcia-Cruz, D.; Fragoso-Herrera, R.; Medina-Lozano, C.--
Confirmation of tyrosine 698 in beta subunit of cGMP phosphodiesterase in patients with retinitis pigmentosa and population of the west of MexicoNunez-Gutierrez, I.C.; Garcia-Cruz, D.; Fragoso-Herrera, R.; Medina-Lozano, C.--
Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndromeGarcia-Cruz, D.; Sanchez-Corona, J.; Nazara, Z.; Garcia-Cruz, M.O.; Figuera, L.E.; Castaneda, V.; Cantu, J.M.--
De novo del(7)(pter?p21.2::p15.2?qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndromeGarcia-Esquivel, L.; Garcia-Cruz, D.; Rivera, H.; Plascencia, M.L.; Cantu, J.M.--
De novo del(7)(pter→p21.2::p15.2→qter) and craniosynostosis. Implications for critical segment assignment in the 7p2 monosomy syndromeGarcia-Esquivel, L.; Garcia-Cruz, D.; Rivera, H.; Plascencia, M.L.; Cantu, J.M.--
Del Xq23 in a mosaic Turner female: Molecular and cytogenetic studiesMesa-Cornejo, V.M.; Garcia-Cruz, D.; Monroy-Jaramillo, N.; Vasquez, A.I.; Davalos, N.O.; Galaviz, C.; Kofman, S.--
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.--
Further clinical delineation in trisomy 1q32 syndromeNuno-Arana, I.; Gonzalez-Garcia, J.R.; Garcia-Cruz, D.--
Further clinical delineation in trisomy 1q32 syndromeNuno-Arana, I.; Gonzalez-Garcia, J.R.; Garcia-Cruz, D.--
Further clinical delineation of fine-lubinsky syndromeCorona-Rivera, J.R.; Lopez-Marure, E.; Garcia-Cruz, D.; Romo-Huerta, C.O.; Rea-Rosas, A.; Orozco-Alatorre, L.G.; Ramirez-Valdivia, J.M.--
Further clinical delineation of fine-lubinsky syndromeCorona-Rivera, J.R.; Lopez-Marure, E.; Garcia-Cruz, D.; Romo-Huerta, C.O.; Rea-Rosas, A.; Orozco-Alatorre, L.G.; Ramirez-Valdivia, J.M.--