Browsing by Author Garcia-Cruz, D.

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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.--
Hereditary multiple benign cystic epithelioma (multiple trichoepithelioma) with onset at early ageCorrea-Cerro, L.S.; Garcia-Cruz, D.; Sarralde, A.; Morales-Peralta, E.; Gonzalez-Mendoza, A.; Sanchez-Corona, J.--
Hereditary multiple benign cystic epithelioma (multiple trichoepithelioma) with onset at early ageCorrea-Cerro, L.S.; Garcia-Cruz, D.; Sarralde, A.; Morales-Peralta, E.; Gonzalez-Mendoza, A.; Sanchez-Corona, J.--
Inherited hypertrichosesGarcia-Cruz, D.; Figuera, L.E.; Cantu, J.M.--
Inherited hypertrichosesGarcia-Cruz, D.; Figuera, L.E.; Cantu, J.M.--
Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly [Deletion interstitielle 6q16.2q22.2 chez un enfant ayant une ectrodactylie]Correa-Cerro, L.; Garcia-Cruz, D.; Diaz-Castanos, L.; Figuera, L.E.; Sanchez-Corona, J.--
Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly [Deletion interstitielle 6q16.2q22.2 chez un enfant ayant une ectrodactylie]Correa-Cerro, L.; Garcia-Cruz, D.; Diaz-Castanos, L.; Figuera, L.E.; Sanchez-Corona, J.--
Mental retardation in a boy with anterior cervical hypertrichosisCorona-Rivera, J.R.; Gonzalez-Abarca, S.; Hernandez-Rocha, J.; Garcia-Cruz, D.; Corona-Rivera, A.--
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.--
Myhre syndrome: First female caseDavalos, N.O.; Garcia-Ortiz, J.E.; Garcia-Cruz, D.; Feria-Velasco, A.; Sanchez-Corona, J.--
Myhre syndrome: First female caseDavalos, N.O.; Garcia-Ortiz, J.E.; Garcia-Cruz, D.; Feria-Velasco, A.; Sanchez-Corona, J.--
On telomere replication and fusion in eukaryotes: Apropos of a case of 45,X/46,X,ter rea(X;X)(p22.3;p22.3)Rivera, H.; Sole, M.T.; Garcia-Cruz, D.--