Browsing by Author Garcia-Cruz, M.O.

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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 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.--
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.--
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.--
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.--
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.--
Schwartz-Jampel syndrome: An atypical form?Figuera, L.E.; Jimenez-Gil, F.J.; Garcia-Cruz, M.O.; Cantu, J.M.--
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.--
Wide clinical spectrum in Zimmermann-Laband syndromeDavalos, I.P.; Brambila-Tapia, A.J.L.; Davalos, N.O.; Duran-Gonzalez, J.; Gonzalez-Mercado, M.G.; Cruz-Ramos, J.A.; Rios-Gonzalez, B.E.; E'Vega, R.; Zavala-Cerna, M.G.; Garcia-Cruz, M.O.; Garcia-Cruz, D.--
Zimmermann-Laband syndrome: Further clinical delineationDavalos, I.P.; Garcia-Cruz, D.; Garcia-Cruz, M.O.; Ramirez-Duenas, M.L.; Solis-Camara, P.; Correa-Cerro, L.S.; Perez-Rulfo, D.; Sanchez-Corona, J.--