Publications by authors named "Sara Frías"

42Publications

Chromosome Instability in Fanconi Anemia: From Breaks to Phenotypic Consequences.

Genes (Basel) 2020 Dec 21;11(12). Epub 2020 Dec 21.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México 04530, Mexico.

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December 2020

Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma.

PLoS One 2020 28;15(12):e0242218. Epub 2020 Dec 28.

Health Effects Genetics Division, Lawrence Livermore National Laboratory, Livermore, California, United States of America.

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January 2021

Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review.

Mol Cytogenet 2020 7;13:42. Epub 2020 Sep 7.

Laboratorio de Citogenética, Departamento de Genética Humana, Instituto Nacional de Pediatría, Mexico City, Mexico.

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September 2020

Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples.

Int J Mol Sci 2019 Oct 23;20(21). Epub 2019 Oct 23.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, 04530 Mexico City, Mexico.

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October 2019

Genomic chaos in peripheral blood lymphocytes of hodgkins lymphoma patients 1 year after ABVD chemotherapy/radiotherapy.

Authors:
Sara Frias

Environ Mol Mutagen 2019 05;60(4):387-388

Laboratorio de Citogenética, INP, Insurgentes Sur 3700-C, 6o. piso, Cd. De Mexico, Mexico.

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May 2019

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

Genes (Basel) 2019 01 10;10(1). Epub 2019 Jan 10.

Subdirección de Hemato-Oncología, Instituto Nacional de Pediatría, Cd. De Mexico, P.O. Box 04530, Mexico.

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January 2019

In Reference to Fanconi Anemia and Laron Syndrome.

Am J Med Sci 2018 06 7;355(6):614-615. Epub 2018 Feb 7.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Ciudad de México, México; Departamento de Medicina Genómica y Toxicología Ambiental, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad de México, México. Electronic address:

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June 2018

DNA Damage as a Driver for Growth Delay: Chromosome Instability Syndromes with Intrauterine Growth Retardation.

Biomed Res Int 2017 12;2017:8193892. Epub 2017 Nov 12.

Laboratorio de Citogenética, Instituto Nacional de Pediatría, Mexico City, Mexico.

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July 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.

Mol Cytogenet 2017 15;10:42. Epub 2017 Nov 15.

Laboratorio de Citogenética, Departamento de Investigación en Genética Humana. Instituto Nacional de Pediatría, Avenida IMAN no. 1, Torre de Investigación, Colonia Insurgentes Cuicuilco, Coyoacán, Ciudad de México, CDMX, Mexico.

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November 2017

Heterogeneous Diagnoses Underlying Radial Ray Anomalies.

Indian J Pediatr 2017 Mar 17;84(3):200-205. Epub 2016 Dec 17.

Departamento de Genética, Instituto Nacional de Perinatología, Montes Urales 800 Col. Lomas Virreyes, C.P 11000, Torre de investigación 2°, Piso, Ciudad de México, CP 11000, Mexico.

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March 2017

Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues.

Genom Data 2016 Sep 24;9:70-7. Epub 2016 Jun 24.

Laboratorio de Citogenética, Depto. de Investigación en Genética Humana, Instituto Nacional de Pediatría, Ciudad de México, México; Unidad de Genética de la Nutrición, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México e Instituto Nacional de Pediatría, Ciudad de México, México.

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September 2016

External ear microRNA expression profiles during mouse development.

Int J Dev Biol 2015 ;59(10-12):497-503

Laboratorio de Citogenética, Depto. de Investigación en Genética Humana, Instituto Nacional de Pediatría, México DF, México.

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November 2016