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Relevancia de la secuenciación de nueva generación en el diagnóstico de cáncer de mama y dos mutaciones descritas por primera vez en población mexicana.
- Published in:
- Salud Pública de México, 2023, v. 65, n. 2, p. 191, doi. 10.21149/14026
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- Publication type:
- Article
Enfermedad de von Willebrand, biología molecular y diagnóstico.
- Published in:
- Cirugía y Cirujanos, 2015, v. 83, n. 3, p. 255, doi. 10.1016/j.circir.2015.05.010
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- Publication type:
- Article
Determinación de los multímeros del factor von Willebrand en población mexicana.
- Published in:
- Cirugía y Cirujanos, 2014, v. 82, n. 6, p. 607
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- Publication type:
- Article
Asociación de la RPCA con mutaciones Leiden y Cambridge del factor V de la coagulación en pacientes mexicanos con tromboflia primaria.
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- Cirugía y Cirujanos, 2010, v. 78, n. 2, p. 131
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- Publication type:
- Article
El diagnóstico de las neuropatías periféricas hereditarias y la genética molecular.
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- Acta Ortopédica Mexicana, 2008, v. 22, n. 4, p. 268
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- Publication type:
- Article
Capillary electrophoresis for the detection of PMP22 gene duplication: Study in Mexican patients.
- Published in:
- Electrophoresis, 2008, v. 29, n. 7, p. 1582, doi. 10.1002/elps.200700614
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- Publication type:
- Article
Prothrombin Time and Coagulation Factor IX as Hemostatic Risk Markers for Legg--Calvé--Perthes Disease.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2023, v. 29, p. 1, doi. 10.1177/10760296221151166
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- Publication type:
- Article
New Genetic Variants of RUNX2 in Mexican Families Cause Cleidocranial Dysplasia.
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- Biology (2079-7737), 2024, v. 13, n. 3, p. 173, doi. 10.3390/biology13030173
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- Publication type:
- Article
Characterization of a group unrelated patients with arthrogryposis multiplex congenita.
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- Jornal de Pediatria, 2016, v. 92, n. 1, p. 58, doi. 10.1016/j.jpedp.2015.10.004
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- Publication type:
- Article
Bone Remodeling and Bone Structural Genes in Legg–Calvé–Perthes Disease: The OPG rs2073618 and IL-6 rs1800795 Are Associated with High Risk in Mexican Patients.
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- DNA & Cell Biology, 2024, v. 43, n. 6, p. 288, doi. 10.1089/dna.2023.0411
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- Publication type:
- Article
Association of Polymorphisms in Estrogen Receptor Genes (ESR1 and ESR2) with Osteoporosis and Fracture—Involvement of Comorbidities and Epistasis.
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- DNA & Cell Biology, 2022, v. 41, n. 4, p. 437, doi. 10.1089/dna.2021.1165
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- Publication type:
- Article
Legg-Calvé-Perthes disease overview.
- Published in:
- 2022
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- Publication type:
- journal article
Association of MTHFR rs1801133 and homocysteine with Legg-Calvé-Perthes disease in Mexican patients.
- Published in:
- 2022
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- Publication type:
- journal article