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Identification of Compound Heterozygous EVC2 Gene Variants in Two Mexican Families with Ellis-van Creveld Syndrome.
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.
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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.
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[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.
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