Browsing by Author Ramirez-Duenas, M.L.

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Assignment of karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridizationAyala-Madrigal, M.L.; Doerr, S.; Ramirez-Duenas, M.L.; Hansmann, I.--
Assignment of karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridizationAyala-Madrigal, M.L.; Doerr, S.; Ramirez-Duenas, M.L.; Hansmann, I.--
Assignment of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridizationAyala-Madrigal, M.L.; Doerr, S.; Ramirez-Duenas, M.L.; Hansmann, I.--
Assignment of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridizationAyala-Madrigal, M.L.; Doerr, S.; Ramirez-Duenas, M.L.; Hansmann, I.--
Floating-Harbor Syndrome, a neuropsychological approachDavalos, I.P.; Figuera, L.E.; Bobadilla, L.; Martinez-Martinez, R.; Matute, E.; Partida, M.G.; Banuelos, L.A.; Ramirez-Duenas, M.L.--
Floating-Harbor Syndrome, a neuropsychological approachDavalos, I.P.; Figuera, L.E.; Bobadilla, L.; Martinez-Martinez, R.; Matute, E.; Partida, M.G.; Banuelos, L.A.; Ramirez-Duenas, M.L.--
Genetically caused deafness: prospective study of 109 children in a special school [Sordera de causa genética: estudio prospectivo en 109 niños de una escuela especial.]Ramirez-Duenas, M.L.; Ramirez-Duenas, M.C.; Matute, E.; Cantu, J.M.--
Genetically caused deafness: prospective study of 109 children in a special school [Sordera de causa gen�tica: estudio prospectivo en 109 ni�os de una escuela especial.]Ramirez-Duenas, M.L.; Ramirez-Duenas, M.C.; Matute, E.; Cantu, J.M.--
Guadalajara camptodactyly type III: A new probably autosomal dominant syndromeFiguera, L.E.; Ramirez-Duenas, M.L.; Davalos, I.P.; Cantu, J.M.--
Guadalajara camptodactyly type III: A new probably autosomal dominant syndromeFiguera, L.E.; Ramirez-Duenas, M.L.; Davalos, I.P.; Cantu, J.M.--
Interstitial 1q42-q44 deletion defined by fish in a short-lived femaleCordova-Fletes, C.; Dominguez Quezada Ma.G.; Diaz-Rodriguez, M.; Ramirez-Duenas, M.L.; Rivera, H.--
Interstitial 1q42-q44 deletion defined by fish in a short-lived femaleCordova-Fletes, C.; Dominguez Quezada Ma.G.; Diaz-Rodriguez, M.; Ramirez-Duenas, M.L.; Rivera, H.--
Silver-Russell syndrome and exclusion of uniparental disomyAyala-Madrigal, M.L.; Shaffer, L.G.; Ramirez-Duenas, M.L.--
Silver-Russell syndrome and exclusion of uniparental disomyAyala-Madrigal, M.L.; Shaffer, L.G.; Ramirez-Duenas, M.L.--
Spondyloepimetaphyseal dysplasia (SEMD) Shohat typeFiguera, L.E.; Ramirez-Duenas, M.L.; Gallegos-Arreola, M.P.; Cantu, J.M.--
Spondyloepimetaphyseal dysplasia (SEMD) Shohat typeFiguera, L.E.; Ramirez-Duenas, M.L.; Gallegos-Arreola, M.P.; Cantu, J.M.--
The Ohdo blepharophimosis syndrome in a Mexican boyFiguera, L.E.; Ramirez-Duenas, M.L.; Rivera, H.--
The Ohdo blepharophimosis syndrome in a Mexican boyFiguera, L.E.; Ramirez-Duenas, M.L.; Rivera, H.--
True hermaphroditism and sequences. Diagnostic implications regarding two cases [Hermafroditismo verdadero y secuencias del cromosoma Y. Implicaciones a propósito de dos casos.]Toscano-Flores, J.J.; Padilla-Gutierrez, J.; Becerra-Solano, L.; Diaz-Rodriguez, M.; Banuelos-Robles, O.; Rivas-Solis, F.; Ramirez-Duenas, M.L.--
True hermaphroditism and sequences. Diagnostic implications regarding two cases [Hermafroditismo verdadero y secuencias del cromosoma Y. Implicaciones a prop�sito de dos casos.]Toscano-Flores, J.J.; Padilla-Gutierrez, J.; Becerra-Solano, L.; Diaz-Rodriguez, M.; Banuelos-Robles, O.; Rivas-Solis, F.; Ramirez-Duenas, M.L.--