Natacci F - Search Results

1

Thyroid findings in pediatric and adult patients with PTEN hamartoma tumor syndrome: A retrospective analysis, and literature review.

Milani D, Dolci A, Muller I, Pavesi MA, Runza L, Kuhn E, Natacci F, Peissel B, Ricci MT, Despini L, Tomasello G, Grossi F, Garrone O, Gambini D. Milani D, et al. Among authors: natacci f. Endocrine. 2023 Jul;81(1):98-106. doi: 10.1007/s12020-023-03313-x. Epub 2023 Jan 23. Endocrine. 2023. PMID: 36690897 Review.

2

Cumming syndrome with heterotaxia, campomelia and absent uterus/fallopian tubes.

Bedeschi MF, Spaccini L, Rizzuti T, Coviello DA, Castorina P, Natacci F, Lalatta F. Bedeschi MF, et al. Among authors: natacci f. Am J Med Genet A. 2005 Jan 30;132A(3):329-30. doi: 10.1002/ajmg.a.30398. Am J Med Genet A. 2005. PMID: 15523630 Review. No abstract available.

3

Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations.

Ruggeri A, Dulcetti F, Miozzo M, Grati FR, Grimi B, Bellato S, Natacci F, Maggi F, Simoni G. Ruggeri A, et al. Among authors: natacci f. Prenat Diagn. 2004 Dec 15;24(12):997-1000. doi: 10.1002/pd.961. Prenat Diagn. 2004. PMID: 15614836

4

The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration.

Nicolini U, Lalatta F, Natacci F, Curcio C, Bui TH. Nicolini U, et al. Among authors: natacci f. Hum Reprod Update. 2004 Nov-Dec;10(6):541-8. doi: 10.1093/humupd/dmh046. Hum Reprod Update. 2004. PMID: 15514017 Review.

5

Developmental abnormalities and cancer predisposition in neurofibromatosis type 1.

Larizza L, Gervasini C, Natacci F, Riva P. Larizza L, et al. Among authors: natacci f. Curr Mol Med. 2009 Jun;9(5):634-53. doi: 10.2174/156652409788488801. Curr Mol Med. 2009. PMID: 19601812 Review.

6

Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.

Giardino D, Finelli P, Russo S, Gottardi G, Rodeschini O, Atza MG, Natacci F, Larizza L. Giardino D, et al. Among authors: natacci f. Am J Med Genet. 2002 Aug 15;111(3):319-23. doi: 10.1002/ajmg.10537. Am J Med Genet. 2002. PMID: 12210331

7

Mental retardation and cardiovascular malformations in NF1 microdeleted patients point to candidate genes in 17q11.2.

Venturin M, Guarnieri P, Natacci F, Stabile M, Tenconi R, Clementi M, Hernandez C, Thompson P, Upadhyaya M, Larizza L, Riva P. Venturin M, et al. Among authors: natacci f. J Med Genet. 2004 Jan;41(1):35-41. doi: 10.1136/jmg.2003.014761. J Med Genet. 2004. PMID: 14729829 Free PMC article. No abstract available.

8

Prenatal manifestation and management of a mother and child affected by spondyloperipheral dysplasia with a C-propeptide mutation in COL2A1: case report.

Bedeschi MF, Bianchi V, Gentilin B, Colombo L, Natacci F, Giglio S, Andreucci E, Trespidi L, Acaia B, Furga AS, Lalatta F. Bedeschi MF, et al. Among authors: natacci f. Orphanet J Rare Dis. 2011 Feb 28;6:7. doi: 10.1186/1750-1172-6-7. Orphanet J Rare Dis. 2011. PMID: 21356074 Free PMC article.

9

FISH characterisation of an identical (16)(p11.2p12.2) tandem duplication in two unrelated patients with autistic behaviour.

Finelli P, Natacci F, Bonati MT, Gottardi G, Engelen JJ, de Die-Smulders CE, Sala M, Giardino D, Larizza L. Finelli P, et al. Among authors: natacci f. J Med Genet. 2004 Jul;41(7):e90. doi: 10.1136/jmg.2003.016311. J Med Genet. 2004. PMID: 15235033 Free PMC article. No abstract available.

10

Clinical follow-up of young adults affected by Williams syndrome: experience of 45 Italian patients.

Bedeschi MF, Bianchi V, Colli AM, Natacci F, Cereda A, Milani D, Maitz S, Lalatta F, Selicorni A. Bedeschi MF, et al. Among authors: natacci f. Am J Med Genet A. 2011 Feb;155A(2):353-9. doi: 10.1002/ajmg.a.33819. Epub 2011 Jan 13. Am J Med Genet A. 2011. PMID: 21271653

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