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F R Grati

Showing results (11-20 of 23) with videos related to

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Cancer Genetics and Cytogenetics|November 7, 2000
Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parametersS M Sirchia, E Sironi, F R Grati, et al.
Case Reports in Genetics|July 22, 2014
Complex variant of Philadelphia translocation involving chromosomes 9, 12, and 22 in a case with chronic myeloid leukaemiaF Malvestiti, C Agrati, S Chinetti, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 14, 2024
Hydatidiform mole identification using non-invasive single-cell sequencing of fetal circulating extravillous trophoblasts isolated from maternal bloodC Mangano, A Doffini, C Forcato, et al.
Placenta|November 24, 2001
Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expressionM Miozzo, F R Grati, G Bulfamante, et al.
Cancer Genetics and Cytogenetics|March 25, 2000
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomasF R Grati, S M Sirchia, I Garagiola, et al.
Placenta|January 25, 2005
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnanciesF R Grati, M Miozzo, B Cassani, et al.
Journal of Medical Genetics|January 30, 2007
Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndromeF R Grati, L Turolla, P D'Ajello, et al.
Human Reproduction (Oxford, England)|April 2, 2010
ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic menE Bonaparte, M Moretti, G M Colpi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 5, 2021
Performance of a targeted cell-free DNA prenatal test for 22q11.2 deletion in a large clinical cohortE Bevilacqua, J C Jani, R Chaoui, et al.
Prenatal Diagnosis|March 16, 2011
Prenatal BACs-on-Beads™ : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosisF Vialard, G Simoni, A Aboura, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Cancer Genetics and Cytogenetics|November 7, 2000
Losses of heterozygosity in endometrial adenocarcinomas: positive correlations with histopathological parametersS M Sirchia, E Sironi, F R Grati, et al.
Case Reports in Genetics|July 22, 2014
Complex variant of Philadelphia translocation involving chromosomes 9, 12, and 22 in a case with chronic myeloid leukaemiaF Malvestiti, C Agrati, S Chinetti, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 14, 2024
Hydatidiform mole identification using non-invasive single-cell sequencing of fetal circulating extravillous trophoblasts isolated from maternal bloodC Mangano, A Doffini, C Forcato, et al.
Placenta|November 24, 2001
Post-zygotic origin of complete maternal chromosome 7 isodisomy and consequent loss of placental PEG1/MEST expressionM Miozzo, F R Grati, G Bulfamante, et al.
Cancer Genetics and Cytogenetics|March 25, 2000
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomasF R Grati, S M Sirchia, I Garagiola, et al.
Placenta|January 25, 2005
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnanciesF R Grati, M Miozzo, B Cassani, et al.
Journal of Medical Genetics|January 30, 2007
Chromosome 11 segmental paternal isodisomy in amniocytes from two fetuses with omphalocoele: new highlights on phenotype-genotype correlations in Beckwith-Wiedemann syndromeF R Grati, L Turolla, P D'Ajello, et al.
Human Reproduction (Oxford, England)|April 2, 2010
ESX1 gene expression as a robust marker of residual spermatogenesis in azoospermic menE Bonaparte, M Moretti, G M Colpi, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|June 5, 2021
Performance of a targeted cell-free DNA prenatal test for 22q11.2 deletion in a large clinical cohortE Bevilacqua, J C Jani, R Chaoui, et al.
Prenatal Diagnosis|March 16, 2011
Prenatal BACs-on-Beads™ : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosisF Vialard, G Simoni, A Aboura, et al.
Pageof 3