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You searched for: Author/Creator Guerneri, Silvana

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1. 13q Deletion and central nervous system anomalies: further insights from karyotype–phenotype analyses of 14 patients. Issue 1 (5th January 2007)

2. Author's reply regarding "Confined placental mosaicism at chorionic villous sampling: risk factors and pregnancy outcome". (1st March 2013)

4. Cytogenetic study in primary myelofibrosis at diagnosis: Clinical and histological association and impact on survival according to WHO 2017 classification in an Italian multicenter series. Issue 1 (4th October 2020)

5. Expression of C19MC miRNAs in HCC associates with stem-cell features and the cancer-testis genes signature. Issue 6 (June 2018)

6. Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome. (27th May 2022)

8. MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion. Issue 8 (24th June 2016)

9. MGMT-Methylated Alleles Are Distributed Heterogeneously Within Glioma Samples Irrespective of IDH Status and Chromosome 10q Deletion. Issue 8 (August 2016)

10. Molecular cytogenetic characterization of a 2q35‐q37 duplication and a 4q35.1‐q35.2 deletion in two cousins: A genotype–phenotype analysis. (6th April 2015)