| 1 | Phenylalanine hydroxylase deficiency treatment and management: A systematic evidence review of the American College of Medical Genetics and Genomics (ACMG) | 2ᵒ autor: Fiesco-Roa, Moises O., Adams, April D., Wong, Lawrence, Jenkins, Gabrielle P., et al. | 2023 | GENETICS IN MEDICINE | WoS-id: 001076916800001
Scopus-id: 2-s2.0-85169781906
| 13 | 14 |
| 2 | Dysmorphology as a Clinical Tool for an Early Diagnosis of Fanconi Anemia | 1ᵉʳ autor: Fiesco-Roa, Moises O., Gomez-Moreno, Paulina G., Espinosa-Curiel, Rubi M., Rodriguez, Alfredo, et al. | 2022 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000791750600006
Scopus-id: 2-s2.0-85130915261
| 1 | 1 |
| 3 | Genotypic spectrum underlying tetrahydrobiopterin metabolism defects: Experience in a single Mexican reference center | Coautor: Fiesco-Roa, M. O., Vela-Amieva, M., Alcantara-Ortigoza, M. A., Ibarra-Gonzalez, I., et al. | 2022 | Frontiers in Genetics | WoS-id: 000877139800001
Scopus-id: 2-s2.0-85140641039
| 5 | 5 |
| 4 | Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability | 1ᵉʳ autor: Fiesco-Roa M.Ó., García-de Teresa B., Leal-Anaya P., van ?t Hek R., et al. | 2022 | Frontiers in Oncology | WoS-id: 000891738100001
Scopus-id: 2-s2.0-85137931063
| 14 | 14 |
| 5 | Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG | Coautor: Fiesco-Roa M.O., Reyes P., García-De Teresa B., Juárez U., et al. | 2022 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000971202400001
Scopus-id: 2-s2.0-85124879348
| 7 | 7 |
| 6 | Inherited Bone Marrow Failure Syndromes: etiology, pathophysiology, diagnosis, and management | 1ᵉʳ autor: Fiesco-Roa, Moises, Monsivais-Orozco, Angelica, Rodriguez, Alfredo, FRIAS, SARA, et al. | 2021 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000681388700005
Scopus-id: 2-s2.0-85110277442
| 0 | 2 |
| 7 | ALG1-CDG Caused by Non-functional Alternative Splicing Involving a Novel Pathogenic Complex Allele | 2ᵒ autor: Fiesco-Roa, Moises O., González-Domínguez C.A., Gomez-Carmona, Samuel, Kleinert-Altamirano A.P.I., et al. | 2021 | Frontiers in Genetics | WoS-id: 000698450800001
Scopus-id: 2-s2.0-85115602741
| 3 | 2 |
| 8 | ALG1-CDG Caused by Non-Functional Alternative Splicing Involving a Novel Pathogenic Complex Allele (vol 12, 744884, 2021) | 2ᵒ autor: Fiesco-Roa, Moises O., Gonzalez-Dominguez, Carlos Alberto, Gomez-Carmona, Samuel, Kleinert-Altamirano A.P.I., et al. | 2021 | Frontiers in Genetics | WoS-id: 000710459000001
Scopus-id: 2-s2.0-85117150206
| 0 | 1 |
| 9 | Microcephaly: diagnostic considerations | 2ᵒ autor: Fiesco-Roa, Moises, Garza-Mayen, Gilda, FRIAS, SARA, Garcia-de Teresa, Benilde | 2020 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000574286600005
Scopus-id: 2-s2.0-85092281719
| 2 | 1 |