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American Journal of Medical Genetics. Part A
|
November 4, 2004
Association of partial trisomy 9p and the Dandy-Walker malformation
Chih-Ping Chen, Chih-Ping Chen, Jin-Chung Shih
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
Prenatal diagnosis of distal 5p deletion syndrome associated with an abnormal first-trimester maternal serum screening result
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
Rapid detection of maternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency thickness and omphalocele on first-trimester prenatal ultrasound
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
Fetal trisomy 18 associated with congenital diaphragmatic hernia, choroid plexus cysts, clenched hands and a maternal origin of the extra chromosome 18
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
False positive non-invasive prenatal testing (NIPT) for partial deletion of chromosome 7q in a pregnancy associated with maternal uterine fibroids and a normal maternal blood cytogenetic result
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
September 12, 2024
Molecular cytogenetic analysis of mosaic 45,X/46,X,r(X) at amniocentesis in a fetus with hydrops fetalis
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
September 12, 2024
Complete cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes is common in mosaic trisomy 20 at amniocentesis with positive conventional cytogenetic analysis and negative chromosomal microarray analysis
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 6, 2025
Difficulty in genetic counseling of prenatally detected de novo 17q12 microdeletion encompassing HNF1B and LHX1 in a fetus with no abnormality on fetal ultrasound
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 6, 2025
First-trimester application of expanded non-invasive prenatal testing in the genetic investigation of fetal 22q11.2 deletion syndrome in a pregnancy conceived by in vitro fertilization and embryo transfer
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
January 10, 2025
Difficulty in genetic counseling of an asymptomatic carrier woman with a de novo 15q13.2q13.3 microdeletion encompassing CHRNA7 and OTUD7A and recurrent 15q13.2q13.3 microdeletion in the fetus
Chih-Ping Chen
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Search research articles
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Showing results (1-10 of 933) with videos related to
Sort By:
Page
of 94
American Journal of Medical Genetics. Part A
|
November 4, 2004
Association of partial trisomy 9p and the Dandy-Walker malformation
Chih-Ping Chen, Chih-Ping Chen, Jin-Chung Shih
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
Prenatal diagnosis of distal 5p deletion syndrome associated with an abnormal first-trimester maternal serum screening result
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
Rapid detection of maternal origin of trisomy 18 by quantitative fluorescent polymerase chain reaction in a fetus associated with increased nuchal translucency thickness and omphalocele on first-trimester prenatal ultrasound
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
Fetal trisomy 18 associated with congenital diaphragmatic hernia, choroid plexus cysts, clenched hands and a maternal origin of the extra chromosome 18
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 14, 2024
False positive non-invasive prenatal testing (NIPT) for partial deletion of chromosome 7q in a pregnancy associated with maternal uterine fibroids and a normal maternal blood cytogenetic result
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
September 12, 2024
Molecular cytogenetic analysis of mosaic 45,X/46,X,r(X) at amniocentesis in a fetus with hydrops fetalis
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
September 12, 2024
Complete cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes is common in mosaic trisomy 20 at amniocentesis with positive conventional cytogenetic analysis and negative chromosomal microarray analysis
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 6, 2025
Difficulty in genetic counseling of prenatally detected de novo 17q12 microdeletion encompassing HNF1B and LHX1 in a fetus with no abnormality on fetal ultrasound
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
March 6, 2025
First-trimester application of expanded non-invasive prenatal testing in the genetic investigation of fetal 22q11.2 deletion syndrome in a pregnancy conceived by in vitro fertilization and embryo transfer
Chih-Ping Chen
Taiwanese Journal of Obstetrics & Gynecology
|
January 10, 2025
Difficulty in genetic counseling of an asymptomatic carrier woman with a de novo 15q13.2q13.3 microdeletion encompassing CHRNA7 and OTUD7A and recurrent 15q13.2q13.3 microdeletion in the fetus
Chih-Ping Chen
Page
of 94