Natacci F - Search Results

1

Norman-Roberts syndrome: characterization of the phenotype in early fetal life.

Natacci F, Bedeschi MF, Righini A, Inverardi F, Rizzuti T, Boschetto C, Triulzi F, Spreafico R, Frassoni C, Lalatta F. Natacci F, et al. Prenat Diagn. 2007 Jun;27(6):568-72. doi: 10.1002/pd.1728. Prenat Diagn. 2007. PMID: 17367103

2

Nasopharyngeal teratoma and diaphragmatic hernia: a non random association?

Natacci F, Moschetta M, Bedeschi MF, Spaccini L, Capelli A, Segni MD, Rizzuti T, Mosca F, Lalatta F. Natacci F, et al. Clin Dysmorphol. 2004 Oct;13(4):255-256. Clin Dysmorphol. 2004. PMID: 15365464

3

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.

4

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.

5

Acro-dermato-ungual-lacrimal-tooth-like syndrome: report of a family with variable expression.

Bedeschi MF, Escande F, Bellini M, Natacci F, Cavallari U, Lalatta F. Bedeschi MF, et al. Among authors: natacci f. Clin Dysmorphol. 2006 Oct;15(4):239-241. doi: 10.1097/01.mcd.0000220618.01144.6d. Clin Dysmorphol. 2006. PMID: 16957482

6

Germline mosaicism in achondroplasia detected in sperm DNA of the father of three affected sibs.

Natacci F, Baffico M, Cavallari U, Bedeschi MF, Mura I, Paffoni A, Setti PL, Baldi M, Lalatta F. Natacci F, et al. Am J Med Genet A. 2008 Mar 15;146A(6):784-6. doi: 10.1002/ajmg.a.32228. Am J Med Genet A. 2008. PMID: 18266238

7

Discordant prenatal phenotype and karyotype of monozygotic twins characterized by the unequal distribution of two cell lines investigated by different methods: a review.

Gentilin B, Guerneri S, Bianchi V, Natacci F, Colombo A, Fogliani R, Fortuna R, Coviello DA, Curcio C, Lalatta F. Gentilin B, et al. Among authors: natacci f. Twin Res Hum Genet. 2008 Jun;11(3):352-6. doi: 10.1375/twin.11.3.352. Twin Res Hum Genet. 2008. PMID: 18498214 Review.

8

Association of syndromic mental retardation with an Xq12q13.1 duplication encompassing the oligophrenin 1 gene.

Bedeschi MF, Novelli A, Bernardini L, Parazzini C, Bianchi V, Torres B, Natacci F, Giuffrida MG, Ficarazzi P, Dallapiccola B, Lalatta F. Bedeschi MF, et al. Among authors: natacci f. Am J Med Genet A. 2008 Jul 1;146A(13):1718-24. doi: 10.1002/ajmg.a.32365. Am J Med Genet A. 2008. PMID: 18512229

9

Recurrence of a severe multiple congenital anomaly syndrome characterized by micrognathia, microtia, cleft palate, and short neck in two siblings.

Natacci F, Bianchi V, Guerneri S, Rizzuti T, Boito S, Gentilin B, Bedeschi MF, Lalatta F. Natacci F, et al. Clin Dysmorphol. 2009 Jan;18(1):45-48. doi: 10.1097/MCD.0b013e328317c867. Clin Dysmorphol. 2009. PMID: 19050404 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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