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

Year Number of Results
2004 1
2005 1
2006 1
2008 4
2009 5
2010 7
2011 5
2012 5
2013 4
2014 2
2015 4
2018 2
2019 2
2020 2
2021 1
2022 1
2024 0

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38 results

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Page 1
The Parma charter of the rights of the newborn.
Bevilacqua G, Corradi M, Donzelli GP, Fanos V, Gianotti D, Magnani C, Orzalesi M, Parmigiani S, Pedrotti D, Salvioli GP. Bevilacqua G, et al. Among authors: magnani c. J Matern Fetal Neonatal Med. 2011 Jan;24(1):171. doi: 10.3109/14767051003792779. Epub 2010 May 12. J Matern Fetal Neonatal Med. 2011. PMID: 20459342 No abstract available.
Disruption of exon-bridging interactions between the minor and major spliceosomes results in alternative splicing around minor introns.
Olthof AM, White AK, Mieruszynski S, Doggett K, Lee MF, Chakroun A, Abdel Aleem AK, Rousseau J, Magnani C, Roifman CM, Campeau PM, Heath JK, Kanadia RN. Olthof AM, et al. Among authors: magnani c. Nucleic Acids Res. 2021 Apr 6;49(6):3524-3545. doi: 10.1093/nar/gkab118. Nucleic Acids Res. 2021. PMID: 33660780 Free PMC article.
FAM111A mutations result in hypoparathyroidism and impaired skeletal development.
Unger S, Górna MW, Le Béchec A, Do Vale-Pereira S, Bedeschi MF, Geiberger S, Grigelioniene G, Horemuzova E, Lalatta F, Lausch E, Magnani C, Nampoothiri S, Nishimura G, Petrella D, Rojas-Ringeling F, Utsunomiya A, Zabel B, Pradervand S, Harshman K, Campos-Xavier B, Bonafé L, Superti-Furga G, Stevenson B, Superti-Furga A. Unger S, et al. Among authors: magnani c. Am J Hum Genet. 2013 Jun 6;92(6):990-5. doi: 10.1016/j.ajhg.2013.04.020. Epub 2013 May 16. Am J Hum Genet. 2013. PMID: 23684011 Free PMC article.
Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.
Maas SM, Shaw AC, Bikker H, Lüdecke HJ, van der Tuin K, Badura-Stronka M, Belligni E, Biamino E, Bonati MT, Carvalho DR, Cobben J, de Man SA, Den Hollander NS, Di Donato N, Garavelli L, Grønborg S, Herkert JC, Hoogeboom AJ, Jamsheer A, Latos-Bielenska A, Maat-Kievit A, Magnani C, Marcelis C, Mathijssen IB, Nielsen M, Otten E, Ousager LB, Pilch J, Plomp A, Poke G, Poluha A, Posmyk R, Rieubland C, Silengo M, Simon M, Steichen E, Stumpel C, Szakszon K, Polonkai E, van den Ende J, van der Steen A, van Essen T, van Haeringen A, van Hagen JM, Verheij JB, Mannens MM, Hennekam RC. Maas SM, et al. Among authors: magnani c. Eur J Med Genet. 2015 May;58(5):279-92. doi: 10.1016/j.ejmg.2015.03.002. Epub 2015 Mar 16. Eur J Med Genet. 2015. PMID: 25792522
38 results