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Genomics|January 20, 1995
Genetic mapping of the spinocerebellar ataxia 2 (SCA2) locus on chromosome 12q23-q24.1A Hernández, C Magariño, S Gispert, et al.
Nature Genetics|July 1, 1993
Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1S Gispert, R Twells, G Orozco, et al.
American Journal of Human Genetics|January 1, 1995
Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneityS Gispert, N Santos, R Damen, et al.
Tissue Antigens|February 17, 2005
Analysis of the functional NFKB1 promoter polymorphism in rheumatoid arthritis and systemic lupus erythematosusG Orozco, E Sánchez, M D Collado, et al.
Rheumatology (Oxford, England)|December 25, 2007
Auto-antibodies, HLA and PTPN22: susceptibility markers for rheumatoid arthritisG Orozco, D Pascual-Salcedo, M A López-Nevot, et al.
The Journal of Rheumatology|February 1, 1992
Trichinosis with severe myopathic involvement mimicking polymyositis. Report of a family outbreakJ Santos Durán-Ortiz, I García-de la Torre, G Orozco-Barocio, et al.
Immunogenetics|December 21, 2006
Patterns of constitutive and IFN-gamma inducible expression of HLA class II molecules in human melanoma cell linesT Rodríguez, R Méndez, A Del Campo, et al.
Human Immunology|June 16, 2015
Analysis of IL10 haplotypes in primary Sjögren's syndrome patients from Western Mexico: Relationship with mRNA expression, IL-10 soluble levels, and autoantibodiesM Vázquez-Villamar, C A Palafox-Sánchez, J F Muñoz-Valle, et al.
Boletin Medico Del Hospital Infantil De Mexico|August 8, 2018
[Meningoencefalitis: etiología infecciosa en pacientes pediátricos de un hospital de referencia]Juan C Lona-Reyes, Ana L Valdez-Núñez, Araceli Cordero-Zamora, et al.
Genetics and Molecular Research : GMR|June 21, 2016
TNFR1-383 A˃C polymorphism association with clinical manifestations in primary Sjögren's syndrome patientsA L Fletes-Rayas, C A Palafox-Sánchez, J F Muñoz-Valle, et al.
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