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Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution.
Murillo-Melo NM, Márquez-Quiróz LC, Gómez R, Orozco L, Mendoza-Caamal E, Tapia-Guerrero YS, Camacho-Mejorado R, Cortés H, López-Reyes A, Santana C, Noris G, Hernández-Hernández O, Cisneros B, Magaña JJ. Murillo-Melo NM, et al. Among authors: marquez quiroz lc. Neuromuscul Disord. 2017 Dec;27(12):1106-1114. doi: 10.1016/j.nmd.2017.09.004. Epub 2017 Sep 21. Neuromuscul Disord. 2017. PMID: 29054426
Oropharyngeal dysphagia in early stages of myotonic dystrophy type 1.
Franco-Guerrero AA, Márquez-Quiroz LC, Valadéz-Jiménez VM, Cortés H, Murillo-Melo NM, Muñoz B, Cisneros B, Magaña JJ. Franco-Guerrero AA, et al. Among authors: marquez quiroz lc. Muscle Nerve. 2019 Jul;60(1):90-95. doi: 10.1002/mus.26485. Epub 2019 May 6. Muscle Nerve. 2019. PMID: 30994189
UPD(14)mat and UPD(14)mat in concomitance with mosaic small supernumerary marker chromosome 14 in two new patients with Temple syndrome.
Garza-Mayén G, Ulloa-Avilés V, Villarroel CE, Navarrete-Meneses P, Lieberman-Hernández E, Abreu-González M, Márquez-Quiroz L, Azotla-Vilchis C, Cifuentes-Goches JC, Del Castillo-Ruiz V, Durán-McKinster C, Pérez-Vera P, Salas-Labadía C. Garza-Mayén G, et al. Eur J Med Genet. 2021 May;64(5):104199. doi: 10.1016/j.ejmg.2021.104199. Epub 2021 Mar 18. Eur J Med Genet. 2021. PMID: 33746039
Silver-Russell syndrome caused by trisomy 11p15.5 due to a derivative X chromosome from a de novo t(X;11) in a Mexican female patient.
Paz-Ramírez M, Muñoz-Martínez LB, Morales-Jiménez AB, Morán-Barroso VF, García-Delgado C, Azotla-Vilchis CN, Márquez-Quiroz LC, Astiazarán MC. Paz-Ramírez M, et al. Among authors: marquez quiroz lc. Clin Dysmorphol. 2022 Apr 1;31(2):94-97. doi: 10.1097/MCD.0000000000000402. Clin Dysmorphol. 2022. PMID: 34750319 No abstract available.