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Chih-Ping Chen

Showing results (71-80 of 933) with videos related to

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Taiwanese Journal of Obstetrics & Gynecology|May 27, 2024
Detection of digynic triploidy in a second-trimester fetus presenting syndactyly, relative macrocephaly, intrauterine growth restriction, cardiomegaly, pericardial effusion, Dandy-Walker malformation, double bubble sign and single umbilical artery on prenatal ultrasound and a false negative non-invasive prenatal testing result in the first trimesterChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|July 5, 2023
Prenatal diagnosis of a 2.14-Mb familial 6q14.1 deletion encompassing the gene of HTR1B with apparently normal phenotypeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|March 14, 2024
Genetic testing using fetal urine at vesicocentesis in case of fetal megacystisChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|March 14, 2024
Molecular cytogenetic characterization of distal 5p deletion syndrome in a fetus with a de novo aberrant chromosome 5 at prenatal diagnosisChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
Prenatal diagnosis of a familial heterozygous pathogenic variant in the PTPN11 gene (c.1510A>G, p.M504V) in a fetus with increased nuchal translucency and pleural effusion and a mother carrier with atypical Noonan syndromeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
High-level mosaicism for 45,X in 45,X/46,XY at amniocentesis in a pregnancy with positive non-invasive prenatal testing for Turner syndrome, a 45,X placenta, hypospadias and unilateral cryptorchidism in the fetus without adverse fetal outcome and perinatal progressive decrease of the 45,X cell lineChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
Postmortem detection of trisomy 18 in a fetus with hydrops fetalis by conventional cytogenetic analysis of cultured umbilical cord cellsChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with perinatal decrease of the trisomy 2 cell line and a favorable fetal outcomeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
High-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with uniparental disomy of chromosome 21, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcomeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2021
Disappearance of the trisomy 8 cell line at long-term follow-up in mosaic trisomy 8 at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen
Pageof 94

Showing results (71-80 of 933) with videos related to

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Pageof 94
Taiwanese Journal of Obstetrics & Gynecology|May 27, 2024
Detection of digynic triploidy in a second-trimester fetus presenting syndactyly, relative macrocephaly, intrauterine growth restriction, cardiomegaly, pericardial effusion, Dandy-Walker malformation, double bubble sign and single umbilical artery on prenatal ultrasound and a false negative non-invasive prenatal testing result in the first trimesterChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|July 5, 2023
Prenatal diagnosis of a 2.14-Mb familial 6q14.1 deletion encompassing the gene of HTR1B with apparently normal phenotypeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|March 14, 2024
Genetic testing using fetal urine at vesicocentesis in case of fetal megacystisChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|March 14, 2024
Molecular cytogenetic characterization of distal 5p deletion syndrome in a fetus with a de novo aberrant chromosome 5 at prenatal diagnosisChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
Prenatal diagnosis of a familial heterozygous pathogenic variant in the PTPN11 gene (c.1510A>G, p.M504V) in a fetus with increased nuchal translucency and pleural effusion and a mother carrier with atypical Noonan syndromeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
High-level mosaicism for 45,X in 45,X/46,XY at amniocentesis in a pregnancy with positive non-invasive prenatal testing for Turner syndrome, a 45,X placenta, hypospadias and unilateral cryptorchidism in the fetus without adverse fetal outcome and perinatal progressive decrease of the 45,X cell lineChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
Postmortem detection of trisomy 18 in a fetus with hydrops fetalis by conventional cytogenetic analysis of cultured umbilical cord cellsChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with perinatal decrease of the trisomy 2 cell line and a favorable fetal outcomeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2025
High-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with uniparental disomy of chromosome 21, perinatal progressive decrease of the trisomy 21 cell line and a favorable fetal outcomeChih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology|September 11, 2021
Disappearance of the trisomy 8 cell line at long-term follow-up in mosaic trisomy 8 at amniocentesis in a pregnancy with a favorable outcomeChih-Ping Chen
Pageof 94