Centro Universitario de los Altos

El Repositorio Institucional del Centro Universitario de los Altos es un acervo digital, construido con la producción intelectual y académica de la comunidad universitaria que lo integra. Es resultado de la actividad cotidiana de alumnos, profesores y administrativos vinculados a las funciones sustantivas de docencia, investigación y gestión.
El objetivo es preservar, dar acceso abierto y difusión a la producción científica y al conocimiento generado, para beneficio común y fomentar su uso de manera ética.

Esta obra está bajo una licencia de Creative Commons Reconocimiento-NoComercial-SinObraDerivada 4.0 Internacional.

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Recent Submissions

Molecular Profiling of Tumor Tissue in Mexican Patients with Colorectal Cancer

Interaction of CCND2, CDKN1A, and POLD3 Variants in Mexican Patients with Colorectal Cancer

Methylation analysis of MIR200 family in Mexican patients with colorectal cancer

Association of the SLC6A4 gene 5HTTLPR polymorphism and ADHD with epilepsy, gestational diabetes, and parental substance abuse in Mexican mestizo children

Isodicentric Y chromosomes and secondary microchromosomes.

MDR1 C3435T Polymorphism in Mexican Children with Acute Lymphoblastic Leukemia and in Healthy Individuals.

Association of LEP and ADIPOQ common variants with colorectal cancer in Mexican patients.

A t(1;9)(q23.3~q25;q34) affecting the ABL1 gene in a biphenotypic leukemia.

Secondary chromosomal changes in 34 Philadelphia-chromosome– positive chronic myelocytic leukemia patients from the Mexican West.

Molecular Characterization of a Patient With 3p Deletion Syndrome and a Review of the Literature

MLH1 and XRCC1 polymorphisms in Mexican patients with colorectal cancer

Increased expression of AML1-a and acquired chromosomal abnormalities in childhood acute lymphoblastic leukemia

Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia.

Capítulo 2. Fisiología de la cognición.

An extra idic(21)(q22.1) in a child with some features of Down’s syndrome

A 45,X sterile male with Yp disguised as 21p

A de novo interstitial 6q deletion in a boy with a split hand malformation

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