Bedeschi MF - Search Results

1

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. 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

2

Molecular characterization of FRAXE-positive subjects with mental impairement in two unrelated Italian families.

Russo S, Selicorni A, Bedeschi MF, Natacci F, Viziello P, Fortuna R, Pagani G, Dalprà L, Larizza L. Russo S, et al. Among authors: bedeschi mf. Am J Med Genet. 1998 Jan 23;75(3):304-8. Am J Med Genet. 1998. PMID: 9475603

3

Maternal chromosome 7 hetero/isodisomy in Silver-Russell syndrome and PEG1 biallelic expression.

Russo S, Bedeschi MF, Cogliati F, Natacci F, Gianotti A, Parini R, Selicorni A, Larizza L. Russo S, et al. Among authors: bedeschi mf. Clin Dysmorphol. 2000 Jul;9(3):157-62. doi: 10.1097/00019605-200009030-00001. Clin Dysmorphol. 2000. PMID: 10955473

4

Biliary atresia and Kabuki syndrome: another case with long-term follow-up.

Selicorni A, Colombo C, Bonato S, Milani D, Giunta AM, Bedeschi MF. Selicorni A, et al. Among authors: bedeschi mf. Am J Med Genet. 2001 May 1;100(3):251. doi: 10.1002/ajmg.1253. Am J Med Genet. 2001. PMID: 11343312 No abstract available.

5

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. Among authors: bedeschi mf. Clin Dysmorphol. 2004 Oct;13(4):255-256. Clin Dysmorphol. 2004. PMID: 15365464

6

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. 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.

7

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. Clin Dysmorphol. 2006 Oct;15(4):239-241. doi: 10.1097/01.mcd.0000220618.01144.6d. Clin Dysmorphol. 2006. PMID: 16957482

8

Rubinstein-Taybi Syndrome: spectrum of CREBBP mutations in Italian patients.

Bentivegna A, Milani D, Gervasini C, Castronovo P, Mottadelli F, Manzini S, Colapietro P, Giordano L, Atzeri F, Divizia MT, Uzielli ML, Neri G, Bedeschi MF, Faravelli F, Selicorni A, Larizza L. Bentivegna A, et al. Among authors: bedeschi mf. BMC Med Genet. 2006 Oct 19;7:77. doi: 10.1186/1471-2350-7-77. BMC Med Genet. 2006. PMID: 17052327 Free PMC article.

9

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. Among authors: bedeschi mf. Prenat Diagn. 2007 Jun;27(6):568-72. doi: 10.1002/pd.1728. Prenat Diagn. 2007. PMID: 17367103

10

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. Among authors: bedeschi mf. 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

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