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ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.
Front Genet. 2021 Sep 9;12:744884. doi: 10.3389/fgene.2021.744884. eCollection 2021.
Front Genet. 2021.
PMID: 34567092
Free PMC article.
Corrigendum: ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele.
González-Domínguez CA, Fiesco-Roa MO, Gómez-Carmona S, Kleinert-Altamirano API, He M, Daniel EJP, Raymond KM, Abreu-González M, Manrique-Hernández S, González-Jaimes A, Salinas-Marín R, Molina-Garay C, Carrillo-Sánchez K, Flores-Lagunes LL, Jiménez-Olivares M, Muñoz-Rivas A, Cruz-Muñoz ME, Ruíz-García M, Freeze HH, Mora-Montes HM, Alaez-Verson C, Martínez-Duncker I.
González-Domínguez CA, et al. Among authors: fiesco roa mo.
Front Genet. 2021 Sep 30;12:777731. doi: 10.3389/fgene.2021.777731. eCollection 2021.
Front Genet. 2021.
PMID: 34659374
Free PMC article.
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Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability.
Fiesco-Roa MÓ, García-de Teresa B, Leal-Anaya P, van 't Hek R, Wegman-Ostrosky T, Frías S, Rodríguez A.
Fiesco-Roa MÓ, et al.
Front Oncol. 2022 Aug 25;12:949435. doi: 10.3389/fonc.2022.949435. eCollection 2022.
Front Oncol. 2022.
PMID: 36091172
Free PMC article.
Review.
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Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG.
Reyes P, García-de Teresa B, Juárez U, Pérez-Villatoro F, Fiesco-Roa MO, Rodríguez A, Molina B, Villarreal-Molina MT, Meléndez-Zajgla J, Carnevale A, Torres L, Frias S.
Reyes P, et al. Among authors: fiesco roa mo.
Int J Mol Sci. 2022 Feb 20;23(4):2334. doi: 10.3390/ijms23042334.
Int J Mol Sci. 2022.
PMID: 35216452
Free PMC article.
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Genotype-phenotype associations in Fanconi anemia: A literature review.
Fiesco-Roa MO, Giri N, McReynolds LJ, Best AF, Alter BP.
Fiesco-Roa MO, et al.
Blood Rev. 2019 Sep;37:100589. doi: 10.1016/j.blre.2019.100589. Epub 2019 Jul 16.
Blood Rev. 2019.
PMID: 31351673
Free PMC article.
Review.
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Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico.
Leal-Anaya P, Kimball TN, Yanez-Felix AL, Fiesco-Roa MÓ, García-de Teresa B, Monsiváis A, Juárez-Velázquez R, Lieberman E, Villarroel C, Yokoyama E, Fernández-Hernández L, Rivera-Osorio A, Sosa D, Ortiz Sandoval MM, López-Santiago N, Frías S, Del Castillo V, Rodríguez A.
Leal-Anaya P, et al. Among authors: fiesco roa mo.
Front Genet. 2024 Jan 24;14:1293929. doi: 10.3389/fgene.2023.1293929. eCollection 2023.
Front Genet. 2024.
PMID: 38327701
Free PMC article.
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Phenylalanine hydroxylase deficiency treatment and management: A systematic evidence review of the American College of Medical Genetics and Genomics (ACMG).
Adams AD, Fiesco-Roa MÓ, Wong L, Jenkins GP, Malinowski J, Demarest OM, Rothberg PG, Hobert JA; ACMG Therapeutics Committee. Electronic address: documents@acmg.net.
Adams AD, et al. Among authors: fiesco roa mo.
Genet Med. 2023 Sep;25(9):100358. doi: 10.1016/j.gim.2022.12.005. Epub 2023 Jul 20.
Genet Med. 2023.
PMID: 37470789
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Genotypic spectrum underlying tetrahydrobiopterin metabolism defects: Experience in a single Mexican reference center.
Vela-Amieva M, Alcántara-Ortigoza MA, Ibarra-González I, González-Del Angel A, Fernández-Hernández L, Guillén-López S, López-Mejía L, Carrillo-Nieto RI, Fiesco-Roa MO, Fernández-Lainez C.
Vela-Amieva M, et al. Among authors: fiesco roa mo.
Front Genet. 2022 Oct 12;13:993612. doi: 10.3389/fgene.2022.993612. eCollection 2022.
Front Genet. 2022.
PMID: 36313470
Free PMC article.
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