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WITHDRAWN: Corrigendum to 'Development of an Italian RM Y-STR haplotype database: results of the 2013 GEFI collaborative exercise' [Forensic. Sci. Int. Genet. 15 (2015) 56-63].
Robino C, Ralf A, Pasino S, De Marchi MR, Ballantyne KN, Barbaro A, Bini C, Carnevali E, Casarino L, Di Gaetano C, Fabbri M, Ferri G, Giardina E, Gonzalez A, Matullo G, Nutini AL, Onofri 5th, Piccinini A, Piglionica M, Ponzano E, Previderè C, Resta N, Scarnicci F, Seidita G, Sorçaburu-Cigliero S, Turrina S, Verzeletti A, Kayser M. Robino C, et al. Among authors: de marchi mr. Forensic Sci Int Genet. 2018 Apr 5:S1872-4973(18)30195-9. doi: 10.1016/j.fsigen.2018.03.014. Online ahead of print. Forensic Sci Int Genet. 2018. PMID: 29627344 No abstract available.
Development of an Italian RM Y-STR haplotype database: Results of the 2013 GEFI collaborative exercise.
Robino C, Ralf A, Pasino S, De Marchi MR, Ballantyne KN, Barbaro A, Bini C, Carnevali E, Casarino L, Di Gaetano C, Fabbri M, Ferri G, Giardina E, Gonzalez A, Matullo G, Nutini AL, Onofri V, Piccinini A, Piglionica M, Ponzano E, Previderè C, Resta N, Scarnicci F, Seidita G, Sorçaburu-Cigliero S, Turrina S, Verzeletti A, Kayser M. Robino C, et al. Among authors: de marchi mr. Forensic Sci Int Genet. 2015 Mar;15:56-63. doi: 10.1016/j.fsigen.2014.10.008. Epub 2014 Oct 14. Forensic Sci Int Genet. 2015. PMID: 25457630 Free article.
Corrigendum to "Development of an Italian RM Y-STR haplotype database: Results of the 2013 GEFI collaborative exercise" [Forensic. Sci. Int. Genet. 15 (2015) 56-63].
Robino C, Ralf A, Pasino S, De Marchi MR, Ballantyne KN, Barbaro A, Bini C, Carnevali E, Casarino L, Di Gaetano C, Fabbri M, Ferri G, Giardina E, Gonzalez A, Matullo G, Nutini AL, Onofri V, Piccinini A, Piglionica M, Ponzano E, Previderè C, Resta N, Scarnicci F, Seidita G, Sorçaburu-Cigliero S, Turrina S, Verzeletti A, Kayser M. Robino C, et al. Among authors: de marchi mr. Forensic Sci Int Genet. 2018 May;34:e23-e24. doi: 10.1016/j.fsigen.2018.01.008. Epub 2018 Feb 7. Forensic Sci Int Genet. 2018. PMID: 29428588 No abstract available.
Unbiased next generation sequencing analysis confirms the existence of autosomal dominant Alport syndrome in a relevant fraction of cases.
Fallerini C, Dosa L, Tita R, Del Prete D, Feriozzi S, Gai G, Clementi M, La Manna A, Miglietti N, Mancini R, Mandrile G, Ghiggeri GM, Piaggio G, Brancati F, Diano L, Frate E, Pinciaroli AR, Giani M, Castorina P, Bresin E, Giachino D, De Marchi M, Mari F, Bruttini M, Renieri A, Ariani F. Fallerini C, et al. Clin Genet. 2014 Sep;86(3):252-7. doi: 10.1111/cge.12258. Epub 2013 Oct 17. Clin Genet. 2014. PMID: 24033287
p53 Arg72Pro and MDM2 309 SNPs in hereditary retinoblastoma.
Epistolato MC, Disciglio V, Livide G, Berchialla P, Mencarelli MA, Marozza A, Amenduni M, Hadjistilianou T, De Francesco S, Acquaviva A, Toti P, Cetta F, Ariani F, De Marchi M, Renieri A, Giachino D. Epistolato MC, et al. J Hum Genet. 2011 Sep;56(9):685-6. doi: 10.1038/jhg.2011.82. Epub 2011 Aug 4. J Hum Genet. 2011. PMID: 21814224 Free article.
A Bg/II polymorphism in the COL4A6 gene.
Renieri A, Galli L, Zhou J, Ballabio A, De Marchi M. Renieri A, et al. Hum Mol Genet. 1994 Oct;3(10):1914. doi: 10.1093/hmg/3.10.1914-a. Hum Mol Genet. 1994. PMID: 7849730 No abstract available.
155 results