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

Year Number of Results
1996 1
2003 1
2005 1
2007 1
2008 1
2009 1
2010 1
2011 3
2012 2
2013 4
2014 5
2015 6
2016 4
2017 1
2018 9
2019 15
2020 8
2021 6
2022 5
2023 5
2024 4

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73 results

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Page 1
Trisomy 13 and 18-Prevalence and mortality-A multi-registry population based analysis.
Goel N, Morris JK, Tucker D, de Walle HEK, Bakker MK, Kancherla V, Marengo L, Canfield MA, Kallen K, Lelong N, Camelo JL, Stallings EB, Jones AM, Nance A, Huynh MP, Martínez-Fernández ML, Sipek A, Pierini A, Nembhard WN, Goetz D, Rissmann A, Groisman B, Luna-Muñoz L, Szabova E, Lapchenko S, Zarante I, Hurtado-Villa P, Martinez LE, Tagliabue G, Landau D, Gatt M, Dastgiri S, Morgan M. Goel N, et al. Among authors: groisman b. Am J Med Genet A. 2019 Dec;179(12):2382-2392. doi: 10.1002/ajmg.a.61365. Epub 2019 Sep 30. Am J Med Genet A. 2019. PMID: 31566869 Free PMC article.
Prenatal diagnosis and prevalence of critical congenital heart defects: an international retrospective cohort study.
Bakker MK, Bergman JEH, Krikov S, Amar E, Cocchi G, Cragan J, de Walle HEK, Gatt M, Groisman B, Liu S, Nembhard WN, Pierini A, Rissmann A, Chidambarathanu S, Sipek A Jr, Szabova E, Tagliabue G, Tucker D, Mastroiacovo P, Botto LD. Bakker MK, et al. Among authors: groisman b. BMJ Open. 2019 Jul 2;9(7):e028139. doi: 10.1136/bmjopen-2018-028139. BMJ Open. 2019. PMID: 31270117 Free PMC article.
Join World Birth Defects Day.
Groisman B, Bermejo-Sánchez E, Romitti PA, Botto LD, Feldkamp ML, Walani SR, Mastroiacovo P. Groisman B, et al. Pediatr Res. 2019 Jul;86(1):3-4. doi: 10.1038/s41390-019-0392-x. Epub 2019 Apr 9. Pediatr Res. 2019. PMID: 30965352 No abstract available.
Identification of copy-number variants in patients with overgrowth disorders.
Parra A, Tenorio-Castano J, Nevado J, Cazalla M, Miranda-Alcaraz L, Gallego-Zazo N, Silván C, Arias P, Pozo-Román J, Ballesta-Martínez MJ, Guillén-Navarro E, Arroyo I, Lotersztein V, Cosentino V, González-Meneses A, Galán E, Rosell J, Ramos F; Spanish OverGrowth Registry Initiative; Lapunzina P. Parra A, et al. Clin Genet. 2024 Nov;106(5):614-624. doi: 10.1111/cge.14596. Epub 2024 Aug 1. Clin Genet. 2024. PMID: 39091142
Genetics and genomic medicine in Argentina.
Vishnopolska SA, Turjanski AG, Herrera Piñero M, Groisman B, Liascovich R, Chiesa A, Marti MA. Vishnopolska SA, et al. Among authors: groisman b. Mol Genet Genomic Med. 2018 Jul 26;6(4):481-91. doi: 10.1002/mgg3.455. Online ahead of print. Mol Genet Genomic Med. 2018. PMID: 30051615 Free PMC article.
Diprosopus: Systematic review and report of two cases.
Bidondo MP, Groisman B, Tardivo A, Tomasoni F, Tejeiro V, Camacho I, Vilas M, Liascovich R, Barbero P. Bidondo MP, et al. Among authors: groisman b. Birth Defects Res A Clin Mol Teratol. 2016 Dec;106(12):993-1007. doi: 10.1002/bdra.23549. Epub 2016 Oct 5. Birth Defects Res A Clin Mol Teratol. 2016. PMID: 27704687 Review.
World Birth Defects Day.
Groisman B, Bidondo MP, Piola A, Tellechea AL, Barbero P, Liascovich R. Groisman B, et al. Arch Argent Pediatr. 2019 Oct 1;117(5):284-285. doi: 10.5546/aap.2019.eng.284. Arch Argent Pediatr. 2019. PMID: 31560482 Free article. English. No abstract available.
[Acheiropodia: first case report in Argentina].
Ormazabal M, Vaccari N, Szulepa R, Bidondo MP, Barbero P, Groisman B. Ormazabal M, et al. Among authors: groisman b. Arch Argent Pediatr. 2015 Oct;113(5):e299-303. doi: 10.5546/aap.2015.e299. Arch Argent Pediatr. 2015. PMID: 26294167 Free article. Spanish.
73 results