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Mutations identified in a cohort of Mexican patients with lysosomal acid lipase deficiency.
Ann Hepatol. 2019 Jul-Aug;18(4):646-650. doi: 10.1016/j.aohep.2018.07.005. Epub 2019 May 9.
Ann Hepatol. 2019.
PMID: 31182375
Free article.
A Novel c.91dupG JAG1 Gene Mutation Is Associated with Early Onset and Severe Alagille Syndrome.
Reyes-de la Rosa ADP, Varela-Fascinetto G, García-Delgado C, Vázquez-Martínez ER, Valencia-Mayoral P, Cerbón M, Morán-Barroso VF.
Reyes-de la Rosa ADP, et al.
Case Rep Genet. 2018 Jun 25;2018:1369413. doi: 10.1155/2018/1369413. eCollection 2018.
Case Rep Genet. 2018.
PMID: 30046498
Free PMC article.
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Nance-Horan syndrome in females due to a balanced X;1 translocation that disrupts the NHS gene: Familial case report and review of the literature.
Gómez-Laguna L, Martínez-Herrera A, Reyes-de la Rosa ADP, García-Delgado C, Nieto-Martínez K, Fernández-Ramírez F, Valderrama-Atayupanqui TY, Morales-Jiménez AB, Villa-Morales J, Kofman S, Cervantes A, Morán-Barroso VF.
Gómez-Laguna L, et al. Among authors: reyes de la rosa adp.
Ophthalmic Genet. 2018 Jan-Feb;39(1):56-62. doi: 10.1080/13816810.2017.1363245. Epub 2017 Sep 18.
Ophthalmic Genet. 2018.
PMID: 28922055
Review.
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Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease.
Márquez-Ávila CS, Vizcaíno-Alarcón A, García-Delgado C, Núñez-Martínez PM, Flores-Ramírez F, Reyes-de la Rosa Adel P, Mendelsberg-Fishbein P, Ibarra-Grajeda D, Medina-Bravo P, Balderrábano-Saucedo N, Esteva-Solsona S, Márquez-Quiróz Ldel C, Flores-Cuevas A, Sánchez-Urbina R, Morales-Jiménez AB, Garibay-Nieto N, Del Bosque-Garza J, Pietropaolo-Cienfuegos D, Gutiérrez-Camacho C, García-Morales L, Morán-Barroso VF.
Márquez-Ávila CS, et al. Among authors: reyes de la rosa adel p.
Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1886-91. doi: 10.1016/j.ijporl.2015.08.038. Epub 2015 Sep 8.
Int J Pediatr Otorhinolaryngol. 2015.
PMID: 26409294
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