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Mosaic 46,XX,der(9)t(9;13)(p24;q12)/46,XX at amniocentesis can be a culture artefact and associated with a favorable fetal outcome
Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.931-932
2023
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Prenatal diagnosis of Down syndrome in a fetus with bilateral pleural effusion in the early second trimester
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.253-256
2024
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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
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.272-275
2024
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Prenatal diagnosis of familial 2p13.1-p12 microduplication in a pregnancy associated with asymptomatic carrier parent
Taiwanese journal of obstetrics & gynecology, 2024-05, Vol.63 (3), p.422-423
2024
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Genetic counseling of non-invasive prenatal testing (NIPT) trisomy 7-positive pregnancies
Taiwanese journal of obstetrics & gynecology, 2024-05, Vol.63 (3), p.293-296
2024
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Prenatal diagnosis of familial 17q11.2 duplication encompassing NF1 in a pregnancy associated with asymptomatic carrier parent
Taiwanese journal of obstetrics & gynecology, 2024-05, Vol.63 (3), p.426-427
2024
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Prenatal diagnosis of familial 266-kb 2q13 microquadruplication encompassing MALL and NPHP1 in a pregnancy associated with asymptomatic carrier parent
Taiwanese journal of obstetrics & gynecology, 2024-05, Vol.63 (3), p.424-425
2024
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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 trimester
Taiwanese journal of obstetrics & gynecology, 2024-05, Vol.63 (3), p.431-434
2024
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Incidental detection of a de novo 16p13.3 microdeletion encompassing PKD1 and a familial Yq11.223 microdeletion encompassing DAZ1 in a fetus with encephalocele on prenatal ultrasound and amniotic band syndrome
Taiwanese journal of obstetrics & gynecology, 2024-05, Vol.63 (3), p.428-430
2024
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False positive non-invasive prenatal testing (NIPT) for trisomy 21 in vanishing twin syndrome pregnancy: A comparison of the NIPT results performed in different gestations
Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.929-930
2023
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Low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable fetal outcome and postnatal decrease of the 45,X cell line
Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.114-115
2024
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Rapid diagnosis of maternal origin of de novo fetal Robertsonian translocation down syndrome of 46,XY,der(13;21)(q10;q10),+21 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with increased nuchal translucency and an abnormal result of first-trimester maternal serum screening
Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.120-121
2024
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Craniorachischisis in a stillbirth associated with maternal smoking
Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.103-104
2024
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Chromosomal abnormalities associated with fetal megacystis
Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.17-18
2024
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Genetic testing using fetal urine at vesicocentesis in case of fetal megacystis
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.257-259
2024
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Fetal trisomy 18 associated with congenital diaphragmatic hernia, choroid plexus cysts, clenched hands and a maternal origin of the extra chromosome 18
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.276-278
2024
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Molecular cytogenetic characterization of distal 5p deletion syndrome in a fetus with a de novo aberrant chromosome 5 at prenatal diagnosis
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.266-269
2024
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Syndromic and single gene disorders associated with fetal pleural effusion (I): Noonan syndrome, RASopathy and congenital lymphatic anomalies
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.174-177
2024
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False positive non-invasive prenatal testing (NIPT) for trisomy 12 in a pregnancy associated with a favorable fetal outcome and normal hemogram in the pregnant woman
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.270-271
2024
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Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.168-173
2024
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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
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.279-280
2024
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Recurrent neural tube defect and craniorachischisis detected in the first trimester and associated with maternal smoking
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.260-262
2024
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Chromosomal abnormalities associated with fetal pleural effusion (I): General overview
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.165-167
2024
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Prenatal diagnosis of distal 5p deletion syndrome associated with an abnormal first-trimester maternal serum screening result
Taiwanese journal of obstetrics & gynecology, 2024-03, Vol.63 (2), p.263-265
2024
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Positive non-invasive prenatal testing for Turner syndrome and low-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy associated with a favorable fetal outcome and a normal 46,XX karyotype at birth
Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.118-119
2024
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