Sensi A - Search Results

1

Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): implication for prenatal diagnosis.

Prontera P, Buldrini B, Aiello V, Gruppioni R, Bonfatti A, Venti G, Ferlini A, Sensi A, Calzolari E, Donti E. Prontera P, et al. Among authors: sensi a. Prenat Diagn. 2006 Jun;26(6):571-6. doi: 10.1002/pd.1463. Prenat Diagn. 2006. PMID: 16683276

2

Prenatal UPD testing survey in Robertsonian translocations.

Gualandi F, Sensi A, Trabanelli C, Falciano F, Bonfatti A, Calzolari E. Gualandi F, et al. Among authors: sensi a. Prenat Diagn. 2000 Jun;20(6):465-8. Prenat Diagn. 2000. PMID: 10861710

3

Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion.

Prontera P, Aiello V, Toschi M, Turci A, Gruppioni R, Buldrini B, Zago S, Bonfatti A, Donti E, Calzolari E, Sensi A. Prontera P, et al. Among authors: sensi a. Genet Couns. 2007;18(3):309-15. Genet Couns. 2007. PMID: 18019372

4

Paracentric inversion of Yq and review of the literature.

Aiello V, Astolfi N, Gruppioni R, Buldrini B, Prontera P, Bonfatti A, Sensi A, Calzolari E. Aiello V, et al. Among authors: sensi a. Genet Couns. 2007;18(4):379-82. Genet Couns. 2007. PMID: 18286818 Review.

5

Familial pericentric inversion of chromosome 18: intrafamilial variability of the recombinant dup(18q).

Prontera P, Buldrini B, Aiello V, Rogaia D, Mencarelli A, Gruppioni R, Bonfatti A, Beltrami N, Donti E, Sensi A. Prontera P, et al. Among authors: sensi a. Genet Couns. 2010;21(1):91-7. Genet Couns. 2010. PMID: 20420035

6

Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype.

Sensi A, Prontera P, Buldrini B, Palma S, Aiello V, Gruppioni R, Calzolari E, Volinia S, Martini A. Sensi A, et al. Am J Med Genet A. 2008 Jan 1;146A(1):110-5. doi: 10.1002/ajmg.a.32059. Am J Med Genet A. 2008. PMID: 18074369

7

Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3.

Calzolari E, Aiello V, Palazzi P, Sensi A, Calzolari S, Orrico D, Calliari L, Holler H, Marzi C, Belli S, Bernardi F, Patracchini P. Calzolari E, et al. Among authors: sensi a. Am J Med Genet. 1996 Apr 9;67(2):154-61. doi: 10.1002/(SICI)1096-8628(19960409)67:2<154::AID-AJMG5>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8723042

8

Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey.

Sensi A, Cavani S, Villa N, Pomponi MG, Fogli A, Gualandi F, Grasso M, Sala E, Pietrobono R, Baldinotti F, Savin E, Ferlini A, Cecconi M, Rossi S, Gallone S, Bellini C, Neri G, Martinoli E, Simi P, Dalprà L, Genuardi M, Dagna-Bricarelli F, Calzolari E. Sensi A, et al. Prenat Diagn. 2004 Aug;24(8):647-52. doi: 10.1002/pd.962. Prenat Diagn. 2004. PMID: 15305356

9

Heteromorphism of human chromosome 18 detected by fluorescent in situ hybridization.

Bonfatti A, Giunta C, Sensi A, Gruppioni R, Rubini M, Fontana F. Bonfatti A, et al. Among authors: sensi a. Eur J Histochem. 1993;37(2):149-54. Eur J Histochem. 1993. PMID: 7688600

10

Heteromorphic variant 18ph+ analyzed by sequential CBG and fluorescence in situ hybridization.

Sensi A, Giunta C, Bonfatti A, Gruppioni R, Rubini M, Fontana F. Sensi A, et al. Hum Hered. 1994 Sep-Oct;44(5):295-7. doi: 10.1159/000154232. Hum Hered. 1994. PMID: 7927359

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