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Identification of Compound Heterozygous EVC2 Gene Variants in Two Mexican Families with Ellis-van Creveld Syndrome.
Negrete-Torres N, Chima-Galán MDC, Sierra-López EA, Sánchez-Ramos J, Álvarez-González I, Reyes-Reali J, Mendoza-Ramos MI, Garrido-Guerrero E, Amato D, Méndez-Catalá CF, Pozo-Molina G, Méndez-Cruz AR. Negrete-Torres N, et al. Among authors: chima galan mdc. Genes (Basel). 2023 Apr 9;14(4):887. doi: 10.3390/genes14040887. Genes (Basel). 2023. PMID: 37107645 Free PMC article.
Wildervanck syndrome: clinical case report.
Chima-Galán MDC, Sánchez-Beltrán NA, García-Ortiz L. Chima-Galán MDC, et al. Arch Argent Pediatr. 2023 Jun 1;121(3):e202202624. doi: 10.5546/aap.2022-02624.eng. Epub 2022 Nov 24. Arch Argent Pediatr. 2023. PMID: 36413195 Free article. English, Spanish.
Interaction of HLA Class II rs9272219 and TMPO rs17028450 (Arg690Cys) Variants Affects Neuromyelitis Optica Spectrum Disorder Susceptibility in an Admixed Mexican Population.
Rosas-Madrigal S, Villarreal-Molina MT, Flores-Rivera J, Rivas-Alonso V, Macias-Kauffer LR, Ordoñez G, Chima-Galán MDC, Acuña-Alonzo V, Macín-Pérez G, Barquera R, Granados J, Valle-Rios R, Corona T, Carnevale A, Romero-Hidalgo S. Rosas-Madrigal S, et al. Among authors: chima galan mdc. Front Genet. 2021 Jul 15;12:647343. doi: 10.3389/fgene.2021.647343. eCollection 2021. Front Genet. 2021. PMID: 34335680 Free PMC article.
[Sjögren-Larsson syndrome: Pediatric case report].
García-Ortiz L, Gómez-López R, Rivera-Pedroza CI, Santillán-Hernández Y, Chima-Galán MDC, Gutiérrez-Salinas J. García-Ortiz L, et al. Among authors: chima galan mdc. Arch Argent Pediatr. 2018 Dec 1;116(6):e773-e777. doi: 10.5546/aap.2018.e773. Arch Argent Pediatr. 2018. PMID: 30457735 Free article. Spanish.