Browsing by Author Nazara, Z.

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Autosomal dominant congenital epiphyseal dysplasia limited to the femoral headsHernandez, A.; Nazara, Z.; Reynoso, M.C.; Lizcano-Gil, L.A.; Lopez, R.; Sarralde, A.; Fragoso, R.--
Autosomal dominant congenital epiphyseal dysplasia limited to the femoral headsHernandez, A.; Nazara, Z.; Reynoso, M.C.; Lizcano-Gil, L.A.; Lopez, R.; Sarralde, A.; Fragoso, R.--
Autosomal dominant congenital macroglossia: Further delineation of the syndromeReynoso, M.C.; Hernandez, A.; Lizcano-Gil, L.A.; Sarralde, A.; Abreu, M.C.; Nazara, Z.; Fragoso, R.--
Autosomal dominant congenital macroglossia: Further delineation of the syndromeReynoso, M.C.; Hernandez, A.; Lizcano-Gil, L.A.; Sarralde, A.; Abreu, M.C.; Nazara, Z.; Fragoso, R.--
Camptodactyly, joint contractures, facial, and skeletal defects: Further delineation of the rozin camptodactyly syndrome [3]García-Ortiz, J.E.; Castaneda-Cisneros, G.; Lopez-Cardona, M.G.; Sanchez-Corona, J.; Patino-García, B.; García-Gonzalez, C.L.; Nazara, Z.; Davalos-Rodriguez, N.; Rodriguez, L.X.; García-Cruz, D.--
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.--
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.--
Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndromeGarcía-Cruz, D.; Sanchez-Corona, J.; Nazara, Z.; García-Cruz, M.O.; Figuera, L.E.; Castaneda, V.; Cantu, J.M.--
Ehlers-Danlos features with progeroid facies and mild mental retardation: Further delineation of the syndromeHernandez, A.; Aguirre-Negrete, M.G.; Gonzalez-Flores, S.; Reynoso-Luna, M.C.; Fragoso, R.; Nazara, Z.; Tapia-Arizmendi, G.; Cantu, J.M.--
Ehlers-Danlos features with progeroid facies and mild mental retardation: Further delineation of the syndromeHernandez, A.; Aguirre-Negrete, M.G.; Gonzalez-Flores, S.; Reynoso-Luna, M.C.; Fragoso, R.; Nazara, Z.; Tapia-Arizmendi, G.; Cantu, J.M.--
Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects A new syndrome?Hernandez, A.; Nazara, Z.; Reynoso, M.C.; Sarralde, A.; Bobadilla, L.; Fragoso, R.--
Generalized osteoporosis in a patient with oculocutaneous hypopigmentation syndrome (OOCHS), without cerebral defects A new syndrome?Hernandez, A.; Nazara, Z.; Reynoso, M.C.; Sarralde, A.; Bobadilla, L.; Fragoso, R.--
Micro-displacement measurement by means of moire patterns, using two Fresnel zone platesGarcía-Ortiz, J.E.; García-Cruz, D.; Davalos, I.P.; Nazara, Z.; García-Cruz, M.O.; Castaneda, V.; Gutierrez-Mendivil, L.; Sanchez-Corona, J.--
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.--
Osteopoikilosis: Report of a familial caseSarralde, A.; Garcia-Cruz, D.; Nazara, Z.; Sanchez-Corona, J.--
Osteopoikilosis: Report of a familial caseSarralde, A.; García-Cruz, D.; Nazara, Z.; Sanchez-Corona, J.--
Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: A distinct autosomal-recessive disorderSarralde, A.; Reynoso, M.C.; Nazara, Z.; Soto, F.; Hernandez, A.--
Prenatal growth retardation, pelvic hypoplasia, and arthrogrypotic changes of lower limbs: A distinct autosomal-recessive disorderSarralde, A.; Reynoso, M.C.; Nazara, Z.; Soto, F.; Hernandez, A.--
SED-brachydactyly and distinctive speech: Report of two new casesGarcia-Cruz, D.; Zafra De La Rosa, G.F.; Sanchez-Corona, J.; Nazara, Z.; Lopez-Cardona, M.G.; Garcia-Ortiz, J.E.; Corona-Rivera, J.R.; Cantu, J.M.--
SED-brachydactyly and distinctive speech: Report of two new casesGarcía-Cruz, D.; Zafra De La Rosa, G.F.; Sanchez-Corona, J.; Nazara, Z.; Lopez-Cardona, M.G.; García-Ortiz, J.E.; Corona-Rivera, J.R.; Cantu, J.M.--