Genesio R - Search Results

1

Invasive prenatal diagnosis during COVID-19 pandemic.

Carbone L, Raffone A, Sarno L, Travaglino A, Saccone G, Gabrielli O, Migliorini S, Sirico A, Genesio R, Castaldo G, Capponi A, Zullo F, Rizzo G, Maruotti GM. Carbone L, et al. Among authors: genesio r. Arch Gynecol Obstet. 2022 Mar;305(3):797-801. doi: 10.1007/s00404-021-06276-4. Epub 2021 Oct 7. Arch Gynecol Obstet. 2022. PMID: 34618213 Free PMC article. No abstract available.

2

Trisomy 18 caused by isochromosome 18p and 18q formation: Is there a milder phenotype?

Maruotti GM, Fabbrini F, Napolitano R, Genesio R, Conti A, Mallia Milanes G, Mazzarelli LL, Martinelli P. Maruotti GM, et al. Among authors: genesio r. Am J Med Genet A. 2011 Jan;155A(1):225-7. doi: 10.1002/ajmg.a.33639. Epub 2010 Dec 10. Am J Med Genet A. 2011. PMID: 21204237 No abstract available.

3

Prenatally diagnosed distal 16p11.2 microdeletion with a novel association with congenital diaphragmatic hernia: a case report.

Genesio R, Maruotti GM, Saccone G, Mormile A, Conti A, Cicatiello R, Sarnataro V, Sirico A, Izzo A, Martinelli P, Nitsch L. Genesio R, et al. Clin Case Rep. 2018 Feb 9;6(4):592-595. doi: 10.1002/ccr3.1369. eCollection 2018 Apr. Clin Case Rep. 2018. PMID: 29636920 Free PMC article.

4

Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency.

Cicatiello R, Pignataro P, Izzo A, Mollo N, Pezone L, Maruotti GM, Sarno L, Sglavo G, Conti A, Genesio R, Nitsch L. Cicatiello R, et al. Among authors: genesio r. Med Sci (Basel). 2019 Feb 27;7(3):40. doi: 10.3390/medsci7030040. Med Sci (Basel). 2019. PMID: 30818867 Free PMC article.

5

First trimester ultrasound features of X-linked Opitz syndrome and early molecular diagnosis: case report and review of the literature.

Sarno L, Maruotti GM, Izzo A, Mazzaccara C, Carbone L, Esposito G, Di Cresce M, Saccone G, Sirico A, Genesio R, Mollo N, Martinelli P, Conti A, Zullo F, Frisso G. Sarno L, et al. Among authors: genesio r. J Matern Fetal Neonatal Med. 2021 Sep;34(18):3089-3093. doi: 10.1080/14767058.2019.1677594. Epub 2019 Oct 21. J Matern Fetal Neonatal Med. 2021. PMID: 31630581 Review.

6

Prenatal BACs-on-Beads™: the prospective experience of five prenatal diagnosis laboratories.

Vialard F, Simoni G, Gomes DM, Abourra A, De Toffol S, Bru F, Martinez Romero MC, Nitsch L, Bouhanna P, Marcato L, Popowski T, Grimi B, Martínez-Conejero JA, Benzacken B, Genesio R, Grati FR. Vialard F, et al. Among authors: genesio r. Prenat Diagn. 2012 Apr;32(4):329-35. doi: 10.1002/pd.2934. Prenat Diagn. 2012. PMID: 22467163

7

Cytogenetic evaluation of isochromosome 17q in posterior fossa tumors of children and correlation with clinical outcome in medulloblastoma. Detection of a novel chromosomal abnormality.

DeChiara C, Borghese A, Fiorillo A, Genesio R, Conti A, D'Amore R, Pettinato G, Varone A, Maggi G. DeChiara C, et al. Among authors: genesio r. Childs Nerv Syst. 2002 Aug;18(8):380-4. doi: 10.1007/s00381-002-0617-9. Epub 2002 Jul 27. Childs Nerv Syst. 2002. PMID: 12192498

8

Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion.

Titomanlio L, Romano A, Conti A, Genesio R, Salerno M, De Brasi D, Nitsch L, Del Giudice E. Titomanlio L, et al. Among authors: genesio r. Am J Med Genet A. 2004 Jun 1;127A(2):197-200. doi: 10.1002/ajmg.a.20667. Am J Med Genet A. 2004. PMID: 15108211

9

Inverted duplication of 15q with terminal deletion in a multiple malformed newborn with intrauterine growth failure and lethal phenotype.

Genesio R, De Brasi D, Conti A, Borghese A, Di Micco P, Di Costanzo P, Paladini D, Ungaro P, Nitsch L. Genesio R, et al. Am J Med Genet A. 2004 Aug 1;128A(4):422-8. doi: 10.1002/ajmg.a.30112. Am J Med Genet A. 2004. PMID: 15264291

10

Altered expression of mitochondrial and extracellular matrix genes in the heart of human fetuses with chromosome 21 trisomy.

Conti A, Fabbrini F, D'Agostino P, Negri R, Greco D, Genesio R, D'Armiento M, Olla C, Paladini D, Zannini M, Nitsch L. Conti A, et al. Among authors: genesio r. BMC Genomics. 2007 Aug 7;8:268. doi: 10.1186/1471-2164-8-268. BMC Genomics. 2007. PMID: 17683628 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

64 results

Search Page