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A de novo phe671eu mutation in the SRY gene in a patient with complete 46,XY gonadal dysgenesis.

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BCR/ABL p210, p190 and p230 fusion genes in 250 Mexican patients with chronic myeloid leukaemia (CML).

Clinical and laboratory haematology·2002

Del Xq23 in a mosaic Turner female: molecular and cytogenetic studies.

Annales de genetique·2002

A t(1;22)(p13;q13) in four children with acute megakaryoblastic leukemia (M7), two with Down syndrome.

Cancer genetics and cytogenetics·2000

Genetic features of Mexican women predisposing to cancer of the uterine cervix.

Human pathology·1999

Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion "hot spot" region.

American journal of medical genetics·1997

Male survivors of childhood cancer and perceptions of sexual dysfunction risk: A report from the Childhood Cancer Survivor Study.

Cancer·2026

T-cell engagers in small cell lung cancer.

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Cancer·2026

Elevated risk of ischemic stroke after invasive cancer diagnosis: A nationwide population-based study.

Cancer·2026

Long-term outcomes and patterns of failure in patients with thymic malignancies treated with surgery and radiation therapy.

Cancer·2026

Diagnostic value of a combined model for acute aortic syndrome based on internal migration of calcification on non-contrast computed tomography.

Journal of thoracic disease·2026

Mechanical properties of the tumor microenvironment: drivers of immunotherapy resistance in solid tumors.

Frontiers in immunology·2026

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Circulation. Cardiovascular interventions·2026

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ACS biomaterials science & engineering·2026

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Journal of biomechanics·2026

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PloS one·2026

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A de novo phe671eu mutation in the SRY gene in a patient with complete 46,XY gonadal dysgenesis.

BCR/ABL p210, p190 and p230 fusion genes in 250 Mexican patients with chronic myeloid leukaemia (CML).

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A t(1;22)(p13;q13) in four children with acute megakaryoblastic leukemia (M7), two with Down syndrome.

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