F. Dulcetti

发表

Chromosome abnormalities investigated by non‐invasive prenatal testing account for approximately 50% of fetal unbalances associated with relevant clinical phenotypes

M. Clementi, G. Simoni, S. De Toffol, 2010, American journal of medical genetics. Part A.

De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches

G. Simoni, S. De Toffol, L. Marcato, 2014, Prenatal diagnosis.

Pure monosomy and pure trisomy of 13q21.2–31.1 consequent to a familial insertional translocation: Exclusion of PCDH9 as the responsible gene for autosomal dominant auditory neuropathy (AUNA1)

Sarah B. Emery, A. Selicorni, G. Simoni, 2009, American journal of medical genetics. Part A.

Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parameters.

G. Pardi, S. Garsia, I. Garagiola, 2000, Cancer genetics and cytogenetics.

Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas.

R. Brusati, A. Bozzetti, I. Garagiola, 2000, Cancer genetics and cytogenetics.

Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi

M. Miozzo, G. Simoni, B. Grimi, 2006, European Journal of Human Genetics.

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

F. Natacci, M. Miozzo, G. Simoni, 2004, Prenatal diagnosis.

Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results

G. Simoni, B. Grimi, E. Gaetani, 2014, Genetics in Medicine.

QF‐PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first‐trimester prenatal diagnoses

G. Simoni, S. De Toffol, L. Marcato, 2013, Prenatal diagnosis.

Three cases with de novo 6q imbalance and variable prenatal phenotype

R. Tenconi, I. Cetin, F. Lalatta, 2005, American journal of medical genetics. Part A.

Quantitative fluorescence-polymerase chain reaction assay for the detection of the duplication of the Charcot Marie Tooth disease type 1A critical region.

E. Bellone, P. Mandich, G. Simoni, 2010, Genetic testing and molecular biomarkers.