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Cuevas-Covarrubias, S.A
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
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Journal Article
A case report of a patient with mucopolysaccharidosis type II
Rivera Vega, M.R, García Vidaña, H, Pacheco Cuéllar, G, Cuevas Covarrubias, S.A
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
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Journal Article
Chromosomal abnormalities in patients with haematologic malignancies in the general hospital of Mexico
Arana Trejo, R.M, del Castillo Moreno, A, Alcalá Carmona, L.G, Madrid Cedillo, V, Kassack Ipiña, J.J, Gutiérrez Romero, M, Cervantes Peredo, A.B, Rozen Fuller, E, Aguilar Martínez, E, Pérez Cabrera, A, Gálvez Galicia, E, Collazo Jaloma, J, Cuevas Covarrubias, S.A
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
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Journal Article
Duo test and aneuploidy detection in women under 35 years of age with high-risk pregnancy at the Hospital General de México
Valdés-Miranda, J.M, Pérez-Cabrera, A, Coronel-Cruz, F, Cuevas-Covarrubias, S
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
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Journal Article
Pharmacokinetics of diclofenac in healthy controls with wild-type phenotype for CYP2C9 shows metabolism variability
Martín-De Saro, M, Amancio-Cassin, O, Urueta-Cuéllar, H, González-Huerta, L, Cuevas-Covarrubias, S
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
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Journal Article
Exome sequencing analysis reveals homozygous GJB2 gene mutation in a Mexican family with profound hearing loss
Martínez-Saucedo, M, Rivera-Vega, M.R, Gonzalez-Huerta, L.M, Urueta-Cuellar, H, Cuevas-Covarrubias, S
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
Published in Revista medica del hospital general de mexico s.s.a (01.04.2017)
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Journal Article
Neuropatía sensitiva autonómica hereditaria tipo IIA: manifestaciones neurológicas y esqueléticas tempranas
Esmer, C, Díaz Zambrano, S, Santos Díaz, M.A, González Huerta, L.M, Cuevas Covarrubias, S.A, Bravo Oro, A
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.04.2014)
Published in Anales de pediatría (Barcelona, Spain : 2003) (01.04.2014)
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Journal Article
Analysis of the VCX3A, VCX2 and VCX3B genes shows that VCX3A gene deletion is not sufficient to result in mental retardation in X-linked ichthyosis: VCX3A gene deletion in XLI without mental retardation
Cuevas-Covarrubias, S.A., González-Huerta, L.M.
Published in British journal of dermatology (1951) (01.03.2008)
Published in British journal of dermatology (1951) (01.03.2008)
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Journal Article
Molecular Analysis of the CYP1B1 Gene: Identification of Novel Truncating Mutations in Patients with Primary Congenital Glaucoma
Messina-Baas, O.M., González-Huerta, L.M., Chima-Galán, C., Kofman-Alfaro, S.H., Rivera-Vega, M.R., Babayán-Mena, I., Cuevas-Covarrubias, S.A.
Published in Ophthalmic research (01.01.2007)
Published in Ophthalmic research (01.01.2007)
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Journal Article
Deletion of Exons 1–5 of the STS Gene Causing X-Linked Ichthyosis
Valdes-Flores, M., Kofman-Alfaro, S.H., Jimenez Vaca, A.L., Cuevas-Covarrubias, S.A.
Published in Journal of investigative dermatology (01.03.2001)
Published in Journal of investigative dermatology (01.03.2001)
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Journal Article