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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2010 3
2011 2
2012 2
2013 9
2014 7
2015 5
2016 5
2017 6
2018 5
2019 5
2020 6
2021 0
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49 results
Results by year
Filters applied: . Clear all The following term was not found in PubMed: Yerlin
Page 1
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.
Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation.
Acosta-Fernández E, Zenteno JC, Chacón-Camacho OF, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Romo-Huerta CO, Zepeda-Romero LC, López-Marure E, Acosta-León J, García-Cruz D, Maciel-Cruz EJ, Corona-Rivera JR. Acosta-Fernández E, et al. Am J Med Genet A. 2020 May;182(5):1223-1229. doi: 10.1002/ajmg.a.61506. Epub 2020 Feb 5. Am J Med Genet A. 2020. PMID: 32022998
SOX2 anophthalmia syndrome and dental anomalies.
Chacon-Camacho OF, Fuerte-Flores BI, Ricardez-Marcial EF, Zenteno JC. Chacon-Camacho OF, et al. Am J Med Genet A. 2015 Nov;167A(11):2830-3. doi: 10.1002/ajmg.a.37277. Epub 2015 Aug 6. Am J Med Genet A. 2015. PMID: 26250054
49 results