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G Simoni

Showing results (151-160 of 159) with videos related to

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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.
Bone|January 29, 2023
Genetic analysis of osteogenesis imperfecta in a large Brazilian cohortA P Holtz, L T Souza, E M Ribeiro, 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.
Minerva Ginecologica|November 6, 2014
A pharmacogenetic-driven approach for controlled ovarian hyperstimulation by FSH treatmentR Colognato, R Aiello, F Dulcetti, 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.
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.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 21, 2012
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011A Novelli, F R Grati, L Ballarati, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
Pageof 16

Showing results (151-160 of 159) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 159 results.
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.
Bone|January 29, 2023
Genetic analysis of osteogenesis imperfecta in a large Brazilian cohortA P Holtz, L T Souza, E M Ribeiro, 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.
Minerva Ginecologica|November 6, 2014
A pharmacogenetic-driven approach for controlled ovarian hyperstimulation by FSH treatmentR Colognato, R Aiello, F Dulcetti, 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.
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.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|January 21, 2012
Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011A Novelli, F R Grati, L Ballarati, et al.
Human Genetics|January 1, 1982
Cytogenetic findings in 4952 prenatal diagnoses. An Italian collaborative studyG Simoni, M Fraccaro, A Arslanian, et al.
Pageof 16