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Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation‐Dependent Probe Amplification.

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Title: Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation‐Dependent Probe Amplification.
Authors: Aguayo‐Orozco, Thania Alejandra1,2 (AUTHOR), Rivera, Horacio2 (AUTHOR), Figuera, Luis E.1,2 (AUTHOR), Esparza‐García, Eduardo3 (AUTHOR), Perea‐Díaz, Francisco Javier1,2 (AUTHOR), Jaloma‐Cruz, Ana Rebeca1 (AUTHOR), Rizo‐de la Torre, Lourdes del Carmen4 (AUTHOR), Domínguez‐Quezada, Ma. Guadalupe1 (AUTHOR) madq67@yahoo.com.mx
Source: Molecular Genetics & Genomic Medicine. Nov2025, Vol. 13 Issue 11, p1-9. 9p.
Database: Academic Search Ultimate
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ISSN:23249269
DOI:10.1002/mgg3.70153