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

Year Number of Results
2002 1
2003 1
2004 1
2006 1
2007 1
2011 1
2013 3
2014 1
2015 1
2016 1
2017 2
2018 3
2019 4
2020 5
2021 1
2022 4
2024 0

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29 results

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Page 1
Frataxin Structure and Function.
Castro IH, Pignataro MF, Sewell KE, Espeche LD, Herrera MG, Noguera ME, Dain L, Nadra AD, Aran M, Smal C, Gallo M, Santos J. Castro IH, et al. Among authors: dain l. Subcell Biochem. 2019;93:393-438. doi: 10.1007/978-3-030-28151-9_13. Subcell Biochem. 2019. PMID: 31939159 Review.
An update on genetic variants of the NKX2-5.
Kolomenski JE, Delea M, Simonetti L, Fabbro MC, Espeche LD, Taboas M, Nadra AD, Bruque CD, Dain L. Kolomenski JE, et al. Among authors: dain l. Hum Mutat. 2020 Jul;41(7):1187-1208. doi: 10.1002/humu.24030. Epub 2020 May 22. Hum Mutat. 2020. PMID: 32369864
Genetics and genomic medicine in Argentina.
Cotignola J, Rozental S, Buzzalino N, Dain L. Cotignola J, et al. Among authors: dain l. Mol Genet Genomic Med. 2019 Apr;7(4):e00571. doi: 10.1002/mgg3.571. Epub 2019 Feb 5. Mol Genet Genomic Med. 2019. PMID: 30724040 Free PMC article.
Genetic characterization of a large cohort of Argentine 21-hydroxylase Deficiency.
Fernández CS, Taboas M, Bruque CD, Benavides-Mori B, Belli S, Stivel M, Oneto A, Pasqualini T, Delea M, Espeche LD, Kolomenski JE, Alba L, Buzzalino N, Dain L. Fernández CS, et al. Among authors: dain l. Clin Endocrinol (Oxf). 2020 Jul;93(1):19-27. doi: 10.1111/cen.14190. Epub 2020 May 3. Clin Endocrinol (Oxf). 2020. PMID: 32289882
Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease.
Delea M, Massara LS, Espeche LD, Bidondo MP, Barbero P, Oliveri J, Brun P, Fabro M, Galain M, Fernández CS, Taboas M, Bruque CD, Kolomenski JE, Izquierdo A, Berenstein A, Cosentino V, Martinoli C, Vilas M, Rittler M, Mendez R, Furforo L, Liascovich R, Groisman B, Rozental S, Dain L, On Behalf Of The Pid Acm-Cc Group. Delea M, et al. Among authors: dain l. Genes (Basel). 2022 Jun 29;13(7):1172. doi: 10.3390/genes13071172. Genes (Basel). 2022. PMID: 35885957 Free PMC article.
Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.
Delea M, Espeche LD, Bruque CD, Bidondo MP, Massara LS, Oliveri J, Brun P, Cosentino VR, Martinoli C, Tolaba N, Picon C, Ponce Zaldua ME, Ávila S, Gutnisky V, Perez M, Furforo L, Buzzalino ND, Liascovich R, Groisman B, Rittler M, Rozental S, Barbero P, Dain L. Delea M, et al. Among authors: dain l. Genes (Basel). 2018 Sep 11;9(9):454. doi: 10.3390/genes9090454. Genes (Basel). 2018. PMID: 30208644 Free PMC article.
29 results