Conti A - Search Results

1

Prenatal diagnosis of 22q11 microdeletion in a fetus with a conotruncal heart defect.

Paladini D, Pacileo G, Palmieri S, Russo MG, Conti A, Piccola BD, Martinelli P. Paladini D, et al. Among authors: conti a. Ultrasound Obstet Gynecol. 1998 Jan;11(1):68-70. doi: 10.1046/j.1469-0705.1998.11010068.x. Ultrasound Obstet Gynecol. 1998. PMID: 9511201 Free article.

2

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. Among authors: conti a. 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

3

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. BMC Genomics. 2007 Aug 7;8:268. doi: 10.1186/1471-2164-8-268. BMC Genomics. 2007. PMID: 17683628 Free PMC article.

4

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: conti a. 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.

5

40 Mb duplication in chromosome band 5p13.1p15.33 with 800 kb terminal deletion in a foetus with mild phenotypic features.

Izzo A, Genesio R, Ronga V, Nocera V, Marullo L, Cicatiello R, Sglavo G, Paladini D, Conti A, Nitsch L. Izzo A, et al. Among authors: conti a. Eur J Med Genet. 2012 Feb;55(2):140-4. doi: 10.1016/j.ejmg.2011.12.004. Epub 2012 Jan 2. Eur J Med Genet. 2012. PMID: 22269966

6

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. Among authors: conti a. 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.

7

Early fetal hydropic changes are associated with moderate dilatation of the brain ventricular system: A clue to a possible link between cervical lymphatic engorgement and ventricular dilatation?

Paladini D, Donarini G, Conti A, Constanza De Angelis L, Witte MH, Genesio R, Bernas M, Bellini T, Boccardo F, Ramenghi LA, Bellini C. Paladini D, et al. Among authors: conti a. Lymphology. 2019;52(1):11-17. Lymphology. 2019. PMID: 31119910

8

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: conti a. 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 Free article. Review.

9

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: conti a. 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

10

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: conti a. 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

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