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Annales De Genetique|January 1, 1981
A screening test for phosphoglycerate kinase deficiencyG Vaca, C Wunsch, C Medina, et al.
Annales De Genetique|January 1, 1987
Dissociation of tdic chromosomes: about a t(15;18)(p11;p11) leading to 18p monosomyL Garcia-Esquivel, H Rivera, J Sanchez-Corona, et al.
Annales De Genetique|January 1, 1979
Some clinical and cytogenetic observations on a ring chromosome 13 (p11 q34)A Hernandez, D Garcia-Cruz, L Plascencia, et al.
Annales De Genetique|January 1, 1981
Simultaneous trisomy 10q24 leads to qter and monosomy 4p16: an example of epistasis at the chromosome levelJ M Cantu, A Hernandez, Z Nazara, et al.
Annales De Genetique|January 1, 1981
A simple screening procedure for glucose phosphate isomerase, phosphofructokinase, aldolase and glyceraldehyde-3-phosphate dehydrogenase deficienciesG Vaca, C Medina, C Wunsch, et al.
Archivos De Investigacion Medica|January 1, 1981
Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited diseaseG Vaca, A Hernández, B Ibarra, et al.
Annales De Biologie Clinique|March 20, 2009
[Study of association of the SNP19 polymorphism of calpain 10 gene with type 2 diabetes in ethnic sub-groups of the Tunisian population: gene-environment interaction]T Baroudi Ouederni, J Sanchez-Corona, H Aounallah Skhiri, et al.
Archivos De Investigacion Medica|January 1, 1978
Galactosemia as a result of galactose-1-phosphate uridyltransferase deficiencyG Vaca, J Sanchez-Corona, C Medina, et al.
The Journal of Rheumatology|May 1, 1997
HLA-DRB1*08 influences the development of disease in Mexican Mestizo with spondyloarthropathyW P Maksymowych, C Gorodezky, A Olivo, et al.
Annals of the Rheumatic Diseases|August 1, 1997
The LMP2 polymorphism is associated with susceptibility to acute anterior uveitis in HLA-B27 positive juvenile and adult Mexican subjects with ankylosing spondylitisW P Maksymowych, G S Jhangri, C Gorodezky, et al.
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