Ana R. Cruz-Jaloma
Guadalajara, JAL, Mexico
Last Updated: 09/26/2026
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Found 17 publications
Mexican Patients With Suspected 22q11.2 Deletion Syndrome: Clinical Characterization and Molecular Findings by Fluorescence In Situ Hybridization and Multiplex Ligation-Dependent Probe Amplification.
Journal: Molecular genetics & genomic medicine
Published: May 19, 2025
Concentration and integrity index of circulating cell-free DNA as a biomarker in pediatric patients with B-ALL.
Journal: Cellular and molecular biology (Noisy-le-Grand, France)
Published: May 14, 2025
CRISPR/Cas9 Edition of the F9 Gene in Human Mesenchymal Stem Cells for Hemophilia B Therapy.
Journal: Life (Basel, Switzerland)
Published: October 14, 2024
Inverse Shifting-PCR Modified by Capillary Electrophoresis for Detecting F8 int22h and int1h Inversions in Severe Hemophilia A Patients and Probable Carriers.
Journal: Life (Basel, Switzerland)
Published: September 12, 2024
Genetic analysis for carrier diagnosis in hemophilia A and B in the Mexican population: 25 years of experience.
Journal: American journal of medical genetics. Part C, Seminars in medical genetics
Published: September 18, 2020
Coronavirus Disease 2019: Hematological Anomalies and Antithrombotic Therapy.
Journal: The Tohoku journal of experimental medicine
Published: August 14, 2020
Molecular genetic diagnosis by next-generation sequencing in a cohort of Mexican patients with haemophilia and report of novel variants.
Journal: Blood cells, molecules & diseases
Published: February 20, 2020
In silico analysis of missense mutations in exons 1-5 of the F9 gene that cause hemophilia B.
Journal: BMC bioinformatics
Published: January 18, 2019
F8 inversions of introns 22 and 1 confer a moderate risk of inhibitors in Mexican patients with severe hemophilia A. Concordance analysis and literature review.
Journal: Blood cells, molecules & diseases
Published: February 10, 2018
Detection of monoclonal B cells in general population from two different regions of Mexico.
Journal: International journal of immunogenetics
Published: May 03, 2017
Molecular thrombophilic profile in Mexican patients with idiopathic recurrent pregnancy loss.
Journal: Genetics and molecular research : GMR
Published: November 04, 2016
Two girls with a de novo Xq rearrangement of paternal origin: t(X;9)(q24;q12) or rea(X)dup q.
Journal: Taiwanese journal of obstetrics & gynecology
Published: September 17, 2015
Last Updated: 09/26/2026