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E Viora

Showing results (31-40 of 41) with videos related to

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Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 15, 2003
Measurement of nasal bone length at 11-14 weeks of pregnancy and its potential role in Down syndrome risk assessmentF Orlandi, C M Bilardo, M Campogrande, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Trisomy 18: Fetal ultrasound findings at different gestational agesE Viora, C Zamboni, G Mortara, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 13, 2015
Accuracy of ultrasound in antenatal diagnosis of placental attachment disordersE Pilloni, M G Alemanno, P Gaglioti, et al.
Minerva Pediatrica|September 15, 1985
[Prenatal diagnosis of thalassemia: experience in Piedmont]V Gabutti, C Amione, C Bessè, et al.
Prenatal Diagnosis|May 1, 1985
Cystic hygroma: prenatal diagnosis and genetic counsellingC Marchese, E Savin, E Dragone, et al.
Journal of Medical Screening|October 27, 2001
Correlations between first and second trimester markers for Down's syndrome screeningM Campogrande, E Viora, G Errante, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 6, 2016
Diagnostic accuracy and cost-effectiveness of different strategies to triage women with adnexal masses: a prospective studyE Piovano, C Cavallero, L Fuso, et al.
Annals of the New York Academy of Sciences|July 15, 2004
Feasibility study for a microchip-based approach for noninvasive prenatal diagnosis of genetic diseasesL Cremonesi, S Galbiati, B Foglieni, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 3, 2010
Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 geneB Gentilin, F Forzano, M F Bedeschi, et al.
American Journal of Medical Genetics. Part A|September 12, 2023
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndromeE Viora-Dupont, A Denommé-Pichon, M Chevarin, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 15, 2003
Measurement of nasal bone length at 11-14 weeks of pregnancy and its potential role in Down syndrome risk assessmentF Orlandi, C M Bilardo, M Campogrande, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Trisomy 18: Fetal ultrasound findings at different gestational agesE Viora, C Zamboni, G Mortara, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|May 13, 2015
Accuracy of ultrasound in antenatal diagnosis of placental attachment disordersE Pilloni, M G Alemanno, P Gaglioti, et al.
Minerva Pediatrica|September 15, 1985
[Prenatal diagnosis of thalassemia: experience in Piedmont]V Gabutti, C Amione, C Bessè, et al.
Prenatal Diagnosis|May 1, 1985
Cystic hygroma: prenatal diagnosis and genetic counsellingC Marchese, E Savin, E Dragone, et al.
Journal of Medical Screening|October 27, 2001
Correlations between first and second trimester markers for Down's syndrome screeningM Campogrande, E Viora, G Errante, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 6, 2016
Diagnostic accuracy and cost-effectiveness of different strategies to triage women with adnexal masses: a prospective studyE Piovano, C Cavallero, L Fuso, et al.
Annals of the New York Academy of Sciences|July 15, 2004
Feasibility study for a microchip-based approach for noninvasive prenatal diagnosis of genetic diseasesL Cremonesi, S Galbiati, B Foglieni, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 3, 2010
Phenotype of five cases of prenatally diagnosed campomelic dysplasia harboring novel mutations of the SOX9 geneB Gentilin, F Forzano, M F Bedeschi, et al.
American Journal of Medical Genetics. Part A|September 12, 2023
Identification of the first homozygous intragenic deletion in the YY1AP1 gene in a consanguineous family: New insights into the phenotypic variability associated with Grange syndromeE Viora-Dupont, A Denommé-Pichon, M Chevarin, et al.
Pageof 5