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Study of genetic variants and their clinical significance in Mexican pediatric patients with epilepsy.
Gene. 2023 Aug 15;877:147565. doi: 10.1016/j.gene.2023.147565. Epub 2023 Jun 12.
Gene. 2023.
PMID: 37315635
Tumorous congenital calcinosis cutis associated with early childhood epileptic encephalopathy with a pathogenic FGF12 gene variant.
Marín-Hernández E, Reyes-Salcedo CA, Cárdenas-Conejo A, Peregrino-Bejarano L, Reyes-Cuayahuitl A, Rayo-Mares D, Siordia-Reyes GA.
Marín-Hernández E, et al. Among authors: reyes cuayahuitl a.
Bol Med Hosp Infant Mex. 2020;77(6):331-336. doi: 10.24875/BMHIM.20000030.
Bol Med Hosp Infant Mex. 2020.
PMID: 33186347
Free article.
English.
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Lipomatosis encefalocraneocutánea: reporte de caso.
Muñoz-Montufar JP, Rayo-Mares JD, Reyes-Cuayahuitl A, Pacheco-Rosas DO, Rangel-Ramírez MP.
Muñoz-Montufar JP, et al. Among authors: reyes cuayahuitl a.
Gac Med Mex. 2017;153(7):915-918. doi: 10.24875/GMM.17002833.
Gac Med Mex. 2017.
PMID: 29414957
Free article.
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