Lucina Morales-Bobadilla

Guadalajara, JAL, Mexico

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 67 publications

MTHFR C677T and A1298C Gene Variants in Patients with Turner Syndrome and Their Mothers.

MTHFR C677T and A1298C Gene Variants in Patients with Turner Syndrome and Their Mothers.

Journal: Genetic testing and molecular biomarkers

Published: April 20, 2026

Fanconi Anemia in Mexican Patients: Molecular Spectrum and Clinical Manifestations in a Case Series.

Fanconi Anemia in Mexican Patients: Molecular Spectrum and Clinical Manifestations in a Case Series.

Journal: International journal of molecular sciences

Published: March 30, 2026

Prenatal Diagnosis of 6q Terminal Deletion Associated with Coffin-Siris Syndrome: Phenotypic Delineation and Review.

Prenatal Diagnosis of 6q Terminal Deletion Associated with Coffin-Siris Syndrome: Phenotypic Delineation and Review.

Journal: Genes

Published: October 16, 2025

Clonal Profiles in a Li-Fraumeni Syndrome Patient With SHH Medulloblastoma: Clonal Evolution, Genomics, and Clinical Implications.

Clonal Profiles in a Li-Fraumeni Syndrome Patient With SHH Medulloblastoma: Clonal Evolution, Genomics, and Clinical Implications.

Journal: Pediatric blood & cancer

Published: September 11, 2025

Spectrum of Germline Cytogenomic Alterations in RB1 in Mexican Patients With Retinoblastoma.

Spectrum of Germline Cytogenomic Alterations in RB1 in Mexican Patients With Retinoblastoma.

Journal: Pediatric blood & cancer

Published: September 10, 2025

Evaluation of NOS3 894G>T (p.Glu298Asp) Variant as Risk Factor for Open Neural Tube Defects in Infants from Western Mexico.

Evaluation of NOS3 894G>T (p.Glu298Asp) Variant as Risk Factor for Open Neural Tube Defects in Infants from Western Mexico.

Journal: Genetic testing and molecular biomarkers

Published: August 29, 2025

ICAM1 778G>A (rs1799969), ADD1 1378G>T (rs4961), NPPA 553T>C (rs5065), and NOS3 894G>T (rs1799983) Variants in Infants with Gastroschisis from Western Mexico.

ICAM1 778G>A (rs1799969), ADD1 1378G>T (rs4961), NPPA 553T>C (rs5065), and NOS3 894G>T (rs1799983) Variants in Infants with Gastroschisis from Western Mexico.

Journal: Genetic testing and molecular biomarkers

Published: May 27, 2025

Retracted: Cowden Syndrome and Oral Lesions: A Case Report Using MLPA.

Retracted: Cowden Syndrome and Oral Lesions: A Case Report Using MLPA.

Journal: The American journal of case reports

Published: February 14, 2025

Cowden Syndrome and Oral Lesions: A Case Report Using MLPA.

Cowden Syndrome and Oral Lesions: A Case Report Using MLPA.

Journal: The American journal of case reports

Published: January 12, 2025

Thanatophoric dysplasia: prevalence, clinical characteristics, and molecular findings in a public hospital from Western Mexico.

Thanatophoric dysplasia: prevalence, clinical characteristics, and molecular findings in a public hospital from Western Mexico.

Journal: Gaceta medica de Mexico

Published: January 01, 2025

De Novo RB1 Germline Variant in Retinoblastoma with Two Subsequent Independent Neoplasms: Case Report and Literature Review.

De Novo RB1 Germline Variant in Retinoblastoma with Two Subsequent Independent Neoplasms: Case Report and Literature Review.

Journal: International journal of molecular sciences

Published: October 14, 2024

Situs Inversus in an Infant With Hypomandibular Faciocranial Syndrome: Clinical Overlap With the Agnathia-Otocephaly Complex.

Situs Inversus in an Infant With Hypomandibular Faciocranial Syndrome: Clinical Overlap With the Agnathia-Otocephaly Complex.

Journal: American journal of medical genetics. Part A

Published: September 01, 2024

Showing 1-12 of 67

Last Updated: 09/26/2026