Browsing by Author Garcia-Cruz, D.

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A de novo interstitial 6q deletion in a boy with a split hand malformationDuran-Gonzalez, J.; Gutierrez-Angulo, M.; Garcia-Cruz, D.; Ayala Ma.D.L.L.; Padilla, M.; Davalos, I.P.--
A de novo interstitial 6q deletion in a boy with a split hand malformationDuran-Gonzalez, J.; Gutierrez-Angulo, M.; Garcia-Cruz, D.; Ayala Ma.D.L.L.; Padilla, M.; Davalos, I.P.--
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 non-sense mutation in the corneodesmosin gene in a Mexican family with hypotrichosis simplex of the scalpDavalos, N.O.; Garcia-Vargas, A.; Pforr, J.; Davalos, I.P.; Picos-Cardenas, V.J.; Garcia-Cruz, D.; Kruse, R.; Figuera, L.E.; Nothen, M.M.; Betz, R.C.--
A variant example of familial Floating-Harbor syndrome?Penaloza, J.M.; Garcia-Cruz, D.; Davalos, I.P.; Davalos, N.O.; Garcia-Cruz, M.O.; Perez-Rulfo, D.; Sanchez-Corona, J.--
Association of late onset spastic paraparesis and dementia: Probably an autosomal dominant form of complicated paraplegiaLizcano-Gil, L.A.; Garcia-Cruz, D.; Bernal-Beltran, M.D.P.; Hernandez, A.--
Bloom syndrome in a Mexican Mestizo girlRivera, H.; Garcia-Cruz, D.; Vaca, G.; Moller, M.; Ramos-Zepeda, R.; Cantu, J.M.--
Bloom syndrome in a Mexican Mestizo girlRivera, H.; Garcia-Cruz, D.; Vaca, G.; Moller, M.; Ramos-Zepeda, R.; Cantu, J.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.--
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.--