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Idalid Cuero‐Quezada

Observed names: Idalid Cuero-Quezada, Idalid Cuero‑Quezada
OpenAlex ID: A5035888520
Acute promyelocytic leukemia with PML/RARA (bcr1, bcr2 and bcr3) transcripts in a pediatric patient
2024 · Jennifer Santana‑Hernández, Alfredo Corona‑Rivera, et al. · Oncology Letters · 5
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MTHFR C677T and A1298C variants in Mexican Mestizo infants with neural tube defects from Western Mexico
2021 · Cristian Irela Aranda‐Sánchez, Lucina Bobadilla‐Morales, et al. · Congenital Anomalies · 4
Frequency of chromosome 22q11.2 deletion among newborns with non-syndromic congenital heart defects from western Mexico
2022 · Gerardo E. Fabián-Morales, Lucina Bobadilla-Morales, et al. · Boletín Médico del Hospital Infantil de México · 2
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Unveiling a pathogenic FANCA gene variant in a Mexican family with Fanconi anemia through next‑generation sequencing
2025 · Idalid Cuero‑Quezada, Sinhue Brukman‑Jiménez, et al. · Experimental and Therapeutic Medicine · 1
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De Novo RB1 Germline Variant in Retinoblastoma with Two Subsequent Independent Neoplasms: Case Report and Literature Review
2024 · José de Jesús Pérez-Becerra, Víctor Ulises Rodríguez-Machuca, et al. · International Journal of Molecular Sciences · 1
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MTHFR 677C>T and 1298A>C Variants in Mothers of Infants with Down Syndrome from Western Mexico
2024 · Yaneris Maibeth Romero-Bolaño, Lucina Bobadilla-Morales, et al. · Genetic Testing and Molecular Biomarkers · 1
Identification of a Small Supernumerary Marker Chromosome in a Turner Syndrome Patient with Karyotype mos 46,X,+mar/45,X
2023 · María Teresa Alejandra González-Rodríguez, Sinhue Alejandro Brukman-Jiménez, et al. · Genes · 1
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Fanconi Anemia in Mexican Patients: Molecular Spectrum and Clinical Manifestations in a Case Series
2026 · Fernando Alexis Flores-Leura, Sinhue Alejandro Brukman-Jiménez, et al. · International Journal of Molecular Sciences
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MTHFR C677T and A1298C Gene Variants in Patients with Turner Syndrome and Their Mothers
2026 · Izabel Maryalexandra Rios-Flores, Lucía Flores-Contreras, et al. · Genetic Testing and Molecular Biomarkers
Evaluation of NOS3 894G>T (p.Glu298Asp) Variant as Risk Factor for Open Neural Tube Defects in Infants from Western Mexico
2025 · Diana Karen Pérez-Alfaro, Lucina Bobadilla-Morales, et al. · Genetic Testing and Molecular Biomarkers
Disferlinopatía: Reporte de un caso infrecuente de distrofia muscular de cinturas asociado a variantes compuestas del gen DYSF identificadas por NGS y análisis de segregación familiar
2024 · Universidad de Guadalajara, Víctor Ulises Rodríguez-Machuca, et al. · Ósmosis Revista Médica Estudiantil
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Works count: 11
Citation count: 15
H-index: 2
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