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Updated: Jan 7, 2026

Candidate Gene Testing in Clinical Cohort Studies with Multiplexed Genotyping and Mass Spectrometry

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Amplificación genómica completa para detectar variantes de un solo gen que causan enfermedades hereditarias

Tania Rojas-Pérez¹, Miguel Ángel Alcántara-Ortigoza², Ariadna González-Del-Ángel²

¹Laboratorio de Investigación y Diagnóstico Molecular, Instituto de Infertilidad y Genética México SC, INGENES, México City, Mexico.

Methods in molecular biology (Clifton, N.J.)

|January 1, 2026

Resumen

No abstract available in PubMed .

Palabras clave:

Amplificación El embrión El genoma Fertilización in vitro Enfermedad monogénica PGT-A y sus derivados PGT-M y sus derivados Acceso a la información

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