Silvia Sanchez

Mexico City, DIF, Mexico

Last Updated: 09/26/2026

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Found 11 publications

Dyskeratosis Congenita with Pigmentary Mosaicism and Hematopoietic Trisomy 9 in a Female Associated with a de novo DKC1 Variant and Markedly Skewed X Chromosome Inactivation.

Dyskeratosis Congenita with Pigmentary Mosaicism and Hematopoietic Trisomy 9 in a Female Associated with a de novo DKC1 Variant and Markedly Skewed X Chromosome Inactivation.

Journal: NPJ genomic medicine

Published: December 15, 2025

The tight bond between Fanconi anemia and aging.

The tight bond between Fanconi anemia and aging.

Journal: Frontiers in aging

Published: November 22, 2025

High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow.

High Burden of Non-Clonal Chromosome Aberrations Before Onset of Detectable Neoplasia in Fanconi Anemia Bone Marrow.

Journal: Cancers

Published: March 16, 2025

Frequent copy number variants in a cohort of Mexican-Mestizo individuals.

Frequent copy number variants in a cohort of Mexican-Mestizo individuals.

Journal: Molecular cytogenetics

Published: November 01, 2022

Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells.

Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells.

Journal: Taiwanese journal of obstetrics & gynecology

Published: December 15, 2020

Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia.

Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia.

Journal: Experimental hematology

Published: July 29, 2020

Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.

Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes.

Journal: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology

Published: March 20, 2019

Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma.

Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma.

Journal: Genes

Published: November 09, 2018

Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.

Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.

Journal: Molecular cytogenetics

Published: January 15, 2018

7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype.

7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype.

Journal: Molecular cytogenetics

Published: September 04, 2017

Persistent genomic instability in peripheral blood lymphocytes from Hodgkin lymphoma survivors.

Persistent genomic instability in peripheral blood lymphocytes from Hodgkin lymphoma survivors.

Journal: Environmental and molecular mutagenesis

Published: December 31, 2011

Showing 1-11 of 11

Last Updated: 09/26/2026