Sensi A - Search Results

1

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

2

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

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

An intermediate phenotype between Hay-Wells and Rapp-Hodgkin syndromes in a patient with a novel P63 mutation: confirmation of a variable phenotypic spectrum with a common aetiology.

Prontera P, Escande F, Cocchi G, Donti E, Martini A, Sensi A. Prontera P, et al. Among authors: sensi a. Genet Couns. 2008;19(4):397-402. Genet Couns. 2008. PMID: 19239083

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

FGFR3 mutation in thanatophoric dysplasia type 1 with bilateral cystic renal dysplasia: coincidence or a new association?

Prontera P, Sensi A, Pilu G, Baldi M, Baffico M, Bonasoni R, Calzolari E. Prontera P, et al. Among authors: sensi a. Genet Couns. 2006;17(4):407-12. Genet Couns. 2006. PMID: 17375526

8

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

9

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

10

Syntenic groups between human chromosome 9 and Indian muntjac chromosomes revealed by ZOO-FISH.

Sensi A, Gruppioni R, Bonfatti A, Rubini M, Giunta C, Fontana F. Sensi A, et al. Eur J Histochem. 1995;39(4):317-20. Eur J Histochem. 1995. PMID: 8835186

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