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Page 1
Genetic analysis of muscular dystrophies: our experience in Mexico.
Folia Neuropathol. 2021;59(3):276-283. doi: 10.5114/fn.2021.109426.
Folia Neuropathol. 2021.
PMID: 34628793
Free article.
Structural and sequence variants in patients with Silver-Russell syndrome or similar features-Curation of a disease database.
Tümer Z, López-Hernández JA, Netchine I, Elbracht M, Grønskov K, Gede LB, Sachwitz J, den Dunnen JT, Eggermann T.
Tümer Z, et al. Among authors: lopez hernandez ja.
Hum Mutat. 2018 Mar;39(3):345-364. doi: 10.1002/humu.23382. Epub 2018 Jan 11.
Hum Mutat. 2018.
PMID: 29250858
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Comparison of mutation profiles in the Duchenne muscular dystrophy gene among populations: implications for potential molecular therapies.
López-Hernández LB, Gómez-Díaz B, Luna-Angulo AB, Anaya-Segura M, Bunyan DJ, Zúñiga-Guzman C, Escobar-Cedillo RE, Roque-Ramírez B, Ruano-Calderón LA, Rangel-Villalobos H, López-Hernández JA, Estrada-Mena FJ, García S, Coral-Vázquez RM.
López-Hernández LB, et al. Among authors: lopez hernandez ja.
Int J Mol Sci. 2015 Mar 9;16(3):5334-46. doi: 10.3390/ijms16035334.
Int J Mol Sci. 2015.
PMID: 25761239
Free PMC article.
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