S. Milani

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.

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.

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.

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.

Frequency of fetal karyotype abnormalities in women undergoing invasive testing in the absence of ultrasound and other high‐risk indications

G. Simoni, F. Maggi, F. Grati, 2016, Prenatal diagnosis.

Determination of Relative Abundance of Biofilm, Genes Associated with it’s Formation and Determination of Genetic Diversity(spa-type) of Staphylococcus Aureus Isolated from Adenoids and Tonsils of Children with Adenoid Hypertrophy

S. Moradi, M. Naghmachi, M. Mirzaii, 2021, Armaghane Danesh.

Incidence of sex chromosome aneuploidy in Northern Italy: 27-year longitudinal study.

A. Gropman, B. Grimi, F. Grati, 2023, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.