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Page 1
A genome-wide association study for survival from a multi-centre European study identified variants associated with COVID-19 risk of death.
Sci Rep. 2024 Feb 6;14(1):3000. doi: 10.1038/s41598-024-53310-x.
Sci Rep. 2024.
PMID: 38321133
Free PMC article.
Validation of a method for noninvasive prenatal testing for fetal aneuploidies risk and considerations for its introduction in the Public Health System.
Gerundino F, Giachini C, Contini E, Benelli M, Marseglia G, Giuliani C, Marin F, Nannetti G, Lisi E, Sbernini F, Periti E, Cordisco A, Colosi E, D'ambrosio V, Mazzi M, Rossi M, Staderini L, Minuti B, Pelo E, Cicatiello R, Maruotti GM, Sglavo G, Conti A, Frusconi S, Pescucci C, Torricelli F.
Gerundino F, et al.
J Matern Fetal Neonatal Med. 2017 Mar;30(6):710-716. doi: 10.1080/14767058.2016.1183633. Epub 2016 May 26.
J Matern Fetal Neonatal Med. 2017.
PMID: 27226231
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Molecular Dissection Using Array Comparative Genomic Hybridization and Clinical Evaluation of An Infertile Male Carrier of An Unbalanced Y;21 Translocation: A Case Report and Review of The Literature.
Orrico A, Marseglia G, Pescucci C, Cortesi A, Piomboni P, Giansanti A, Gerundino F, Ponchietti R.
Orrico A, et al. Among authors: gerundino f.
Int J Fertil Steril. 2016 Jan-Mar;9(4):581-5. doi: 10.22074/ijfs.2015.4619. Epub 2015 Dec 23.
Int J Fertil Steril. 2016.
PMID: 26985348
Free PMC article.
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16p11.2 de novo microdeletion encompassing SRCAP gene in a patient with speech impairment, global developmental delay and behavioural problems.
Gerundino F, Marseglia G, Pescucci C, Pelo E, Benelli M, Giachini C, Federighi B, Antonelli C, Torricelli F.
Gerundino F, et al.
Eur J Med Genet. 2014 Nov-Dec;57(11-12):649-53. doi: 10.1016/j.ejmg.2014.09.009.
Eur J Med Genet. 2014.
PMID: 25451714
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372 kb microdeletion in 18q12.3 causing SETBP1 haploinsufficiency associated with mild mental retardation and expressive speech impairment.
Marseglia G, Scordo MR, Pescucci C, Nannetti G, Biagini E, Scandurra V, Gerundino F, Magi A, Benelli M, Torricelli F.
Marseglia G, et al. Among authors: gerundino f.
Eur J Med Genet. 2012 Mar;55(3):216-21. doi: 10.1016/j.ejmg.2012.01.005. Epub 2012 Jan 25.
Eur J Med Genet. 2012.
PMID: 22333924
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