Arce-Gonzalez R - Search Results

1

Expansion of the clinical ocular spectrum of Wolfram Syndrome in a family carrying a novel WFS1 gene deletion.

Chacón-Camacho O, Arce-Gonzalez R, Granillo-Alvarez M, Flores-Limas S, Ramírez M, Zenteno JC. Chacón-Camacho O, et al. Ophthalmic Genet. 2013 Dec;34(4):243-8. doi: 10.3109/13816810.2012.755631. Epub 2013 Feb 1. Ophthalmic Genet. 2013. PMID: 23373429

2

Identification and expression analysis of a novel intragenic EFNB1 mutation causing craniofrontonasal syndrome.

Chacon-Camacho OF, Arce-Gonzalez R, Villegas-Ruiz V, Pelcastre-Luna E, Uría-Gómez CE, Granillo-Alvarez M, Zenteno JC. Chacon-Camacho OF, et al. Meta Gene. 2013 Nov 28;2:25-31. doi: 10.1016/j.mgene.2013.11.001. eCollection 2014 Dec. Meta Gene. 2013. PMID: 25606386 Free PMC article.

3

Extensive genic and allelic heterogeneity underlying inherited retinal dystrophies in Mexican patients molecularly analyzed by next-generation sequencing.

Zenteno JC, García-Montaño LA, Cruz-Aguilar M, Ronquillo J, Rodas-Serrano A, Aguilar-Castul L, Matsui R, Vencedor-Meraz CI, Arce-González R, Graue-Wiechers F, Gutiérrez-Paz M, Urrea-Victoria T, de Dios Cuadras U, Chacón-Camacho OF. Zenteno JC, et al. Mol Genet Genomic Med. 2020 Jan;8(1):10.1002/mgg3.1044. doi: 10.1002/mgg3.1044. Epub 2019 Nov 17. Mol Genet Genomic Med. 2020. PMID: 31736247 Free PMC article.

4

Newborn transient patterned hyperpigmentation and anophthalmia.

Chacón Camacho OF, Arce-González R, Rodríguez Uribe G. Chacón Camacho OF, et al. Bol Med Hosp Infant Mex. 2020;77(3):146-148. doi: 10.24875/BMHIM.19000191. Bol Med Hosp Infant Mex. 2020. PMID: 32496470 English.

5

Exome sequencing identifies a SREBF1 recurrent ARG557CYS mutation as the cause of hereditary mucoepithelial dysplasia in a family with high clinical variability.

Chacon-Camacho OF, Arce-Gonzalez R, Ordaz-Robles T, Perezpeña-Diazconti M, Nava-Castañeda A, Zenteno JC. Chacon-Camacho OF, et al. Among authors: arce gonzalez r. Am J Med Genet A. 2020 Nov;182(11):2773-2777. doi: 10.1002/ajmg.a.61849. Epub 2020 Sep 9. Am J Med Genet A. 2020. PMID: 32902915

6

Novel CHRDL1 mutation causing X-linked megalocornea in a family with mild anterior segment manifestations in carrier females.

Arce-Gonzalez R, Chacon-Camacho OF, Navas-Perez A, Gonzalez-Gonzalez MC, Martinez-Aguilar A, Zenteno JC. Arce-Gonzalez R, et al. Ophthalmic Genet. 2022 Apr;43(2):224-229. doi: 10.1080/13816810.2021.2002917. Epub 2021 Nov 29. Ophthalmic Genet. 2022. PMID: 34844512

7

Clinical-genetic findings in a group of subjects with macular dystrophies due to mutations in rare inherited retinopathy genes.

Zenteno JC, Arce-Gonzalez R, Matsui R, Lopez-Bolaños A, Montes L, Martinez-Aguilar A, Chacon-Camacho OF. Zenteno JC, et al. Among authors: arce gonzalez r. Graefes Arch Clin Exp Ophthalmol. 2023 Feb;261(2):353-365. doi: 10.1007/s00417-022-05786-4. Epub 2022 Aug 10. Graefes Arch Clin Exp Ophthalmol. 2023. PMID: 35947183

8

A novel homozygous ZNF469 variant causing brittle cornea syndrome is associated with corneal ectasias in heterozygous carriers.

Arce-González R, Chacon-Camacho OF, Ordoñez-Labastida V, Graue-Hernandez EO, Navas-Pérez A, Zenteno JC. Arce-González R, et al. Int Ophthalmol. 2023 Mar;43(3):807-815. doi: 10.1007/s10792-022-02481-5. Epub 2022 Sep 1. Int Ophthalmol. 2023. PMID: 36048286

9

Case report: Disease phenotype associated with simultaneous biallelic mutations in ABCA4 and USH2A due to uniparental disomy of chromosome 1.

Villafuerte-De la Cruz R, Chacon-Camacho OF, Rodriguez-Martinez AC, Xilotl-De Jesus N, Arce-Gonzalez R, Rodriguez-De la Torre C, Valdez-Garcia JE, Rojas-Martinez A, Zenteno JC. Villafuerte-De la Cruz R, et al. Among authors: arce gonzalez r. Front Genet. 2022 Aug 16;13:949437. doi: 10.3389/fgene.2022.949437. eCollection 2022. Front Genet. 2022. PMID: 36051698 Free PMC article.

10

Learning from history in the midst of the COVID-19: epidemics/pandemics of antiquity up to the fall of the Western Roman Empire.

Chacón-Camacho ÓF, Arce-González R, Zenteno JC, Granillo MT. Chacón-Camacho ÓF, et al. Among authors: arce gonzalez r. Bol Med Hosp Infant Mex. 2023;80(5):269-278. doi: 10.24875/BMHIM.22000147. Bol Med Hosp Infant Mex. 2023. PMID: 37963299 Free article. English.

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