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

Year Number of Results
2002 1
2006 1
2010 1
2011 1
2012 3
2013 1
2014 4
2015 1
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2020 1
2021 2
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2024 1

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Page 1
New Genetic Variants of RUNX2 in Mexican Families Cause Cleidocranial Dysplasia.
Toral López J, Gómez Martinez S, Rivera Vega MDR, Hernández-Zamora E, Cuevas Covarrubias S, Ibarra Castrejón BA, González Huerta LM. Toral López J, et al. Among authors: gonzalez huerta lm. Biology (Basel). 2024 Mar 8;13(3):173. doi: 10.3390/biology13030173. Biology (Basel). 2024. PMID: 38534443 Free PMC article.
Discordant retinoblastoma in monozygotic twins due to deletion of 13q14.
Messina-Baas OM, Arroyo-Yllanes ME, Pérez-Pérez JF, González-Huerta LM, Cuevas-Covarrubias SA. Messina-Baas OM, et al. Among authors: gonzalez huerta lm. Eur J Ophthalmol. 2014 Nov-Dec;24(6):968-71. doi: 10.5301/ejo.5000447. Epub 2014 Feb 18. Eur J Ophthalmol. 2014. PMID: 24557757
Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy.
Martin-de Saro M, Compean Z, Aguilar K, González-Huerta LM, Plaza-Benhumea L, Messina-Baas O, Cuevas-Covarrubiass SA. Martin-de Saro M, et al. Among authors: gonzalez huerta lm. Mol Syndromol. 2021 Aug;12(5):305-311. doi: 10.1159/000516058. Epub 2021 Jul 20. Mol Syndromol. 2021. PMID: 34602958 Free PMC article.
Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment.
Loeza-Becerra F, Rivera-Vega Mdel R, Martínez-Saucedo M, Gonzalez-Huerta LM, Urueta-Cuellar H, Berrruecos-Villalobos P, Cuevas-Covarrubias S. Loeza-Becerra F, et al. Among authors: gonzalez huerta lm. Int J Pediatr Otorhinolaryngol. 2014 Jul;78(7):1057-60. doi: 10.1016/j.ijporl.2014.04.002. Epub 2014 Apr 12. Int J Pediatr Otorhinolaryngol. 2014. PMID: 24774219
18 results