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Annales De Genetique|January 1, 1992
fra(1) (p11), fra(1) (q22) and r(1) (p11q22) in a retarded girlM L Ramírez-Dueñas, G J GonzálezClinical Genetics|December 1, 1996
Silver-Russell syndrome and exclusion of uniparental disomyM L Ayala-Madrigal, L G Shaffer, M L Ramírez-DueñasClinical Genetics|January 1, 1992
Severe Silver-Russell syndrome and translocation (17;20) (q25;q13)M L Ramírez-Dueñas, C Medina, R Ocampo-Campos, et al.Archivos De Investigacion Medica|October 1, 1990
[Genetically caused deafness: prospective study of 109 children in a special school]M L Ramírez-Dueñas, M C Ramírez-Dueñas, E Matute, et al.Clinical Dysmorphology|October 29, 2002
Guadalajara camptodactyly type III: a new probably autosomal dominant syndromeL E Figuera, M L Ramírez-Dueñas, I P Dávalos, et al.Ginecologia Y Obstetricia De Mexico|January 31, 2002
[Gestational diabetes mellitus and congenital malformations]B Lazalde, R Sánchez-Urbina, J E García de Alba, et al.American Journal of Medical Genetics|July 1, 1994
Spondyloepimetaphyseal dysplasia (SEMD) Shohat typeL E Figuera, M L Ramírez-Dueñas, M P Gallegos-Arreola, et al.Genetic Counseling (Geneva, Switzerland)|June 21, 2008
Interstitial 1q42-q44 deletion defined by FISH in a short-lived femaleC Córdova-Fletes, M G Domínguez, M Díaz-Rodríguez, et al.Clinical Genetics|January 1, 1993
Guadalajara camptodactyly syndrome type I. A corroborative familyL E Figuera, M L Ramírez-Dueñas, D García-Cruz, et al.Cancer Genetics and Cytogenetics|October 23, 1997
Two different Philadelphia chromosomes in a cell line from an AML-M0 patientJ R González García, O M Garcés Ruíz, J L Delgado Lamas, et al.Pageof 2