Pilar Salas-Carrasco
Huelva, AN, Spain
Last Updated: 09/26/2026
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Found 11 publications
Findings in Chromosomal Microarray Analysis during Prenatal Diagnosis in High-Risk Individuals.
Journal: Molecular syndromology
Published: September 16, 2024
Considerations for hereditary breast and ovarian cancer syndrome molecular diagnosis: experience from the clinical practice.
Journal: Breast cancer research and treatment
Published: August 14, 2024
Diversity of oncopharmacogenetic profile within Spanish population.
Journal: Pharmacogenetics and genomics
Published: March 15, 2024
Contingent prenatal screening for frequent aneuploidies with cell-free fetal DNA analysis.
Journal: Taiwanese journal of obstetrics & gynecology
Published: March 04, 2021
Unusual clinical presentation and new mutation in a case of triple A syndrome.
Journal: Endocrinologia, diabetes y nutricion
Published: December 12, 2020
Clinical and molecular characterization of hereditary spastic paraplegia in a spanish Southern region.
Journal: The International journal of neuroscience
Published: October 16, 2020
Genetics and biochemistry of familial hypercholesterolemia in Southwest of the Iberian Peninsula.
Journal: Clinica e investigacion en arteriosclerosis : publicacion oficial de la Sociedad Espanola de Arteriosclerosis
Published: May 02, 2020
Noonan syndrome: Severe phenotype and PTPN11 mutations.
Journal: Medicina clinica
Published: January 11, 2018
Language and Cognitive Impairment Associated with a Novel p.Cys63Arg Change in the MED13L Transcriptional Regulator.
Journal: Molecular syndromology
Published: October 17, 2017
Genetic predisposition to childhood cancer
Journal: Anales de pediatria (Barcelona, Spain : 2003)
Published: January 19, 2017
The role of CDKN2A/B deletions in pediatric acute lymphoblastic leukemia.
Journal: Pediatric hematology and oncology
Published: December 15, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026