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High-Performance and Highly Durable Inverted Organic Photovoltaics Embedding Solution-Processable Vanadium Oxides as an Interfacial Hole-Transporting Layer

Advanced materials (Weinheim), 2011-09, Vol.23 (33), p.3859-3863

2011

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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

Chen, Chih-Ping

2024

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Carbon Nanodot Additives Realize High‐Performance Air‐Stable p–i–n Perovskite Solar Cells Providing Efficiencies of up to 20.2

Advanced energy materials, 2018-12, Vol.8 (34), p.n/a

2018

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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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

2024

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Detection of 45,X/46,X,r(X)(p11.3q22.1) in a 17-year-old girl with secondary amenorrhea, short stature and normal intelligence

Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.111-113

Chen, Chih-Ping

2024

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Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly

Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.105-107

Chen, Chih-Ping

2024

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Chromosomal abnormalities associated with fetal megacystis

Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.17-18

Chen, Chih-Ping

2024

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Syndromic and single gene disorders associated with fetal megacystis (I): Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS)

Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.19-21

Chen, Chih-Ping

2024

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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

Chen, Chih-Ping

2024

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Rapid diagnosis of maternal origin of fetal trisomy 13 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with young maternal age and omphalocele on prenatal ultrasound

Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.108-110

Chen, Chih-Ping

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

Chen, Chih-Ping

2024

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Mosaicism for trisomy 13 in a single colony at amniocentesis in a pregnancy associated with a favorable outcome

Taiwanese journal of obstetrics & gynecology, 2024-01, Vol.63 (1), p.122-124

Chen, Chih-Ping

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

Chen, Chih-Ping

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

Chen, Chih-Ping

2023

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Identification of a familial balanced chromosomal rearrangement in a couple presenting with recurrent pregnancy loss

Taiwanese journal of obstetrics & gynecology, 2023-11, Vol.62 (6), p.925-926

Chen, Chih-Ping

2023

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High-Performance and Highly Durable Inverted Organic Photovoltaics Embedding Solution-Processable Vanadium Oxides as an Interfacial Hole-Transporting Layer

Prenatal diagnosis of Down syndrome in a fetus with bilateral pleural effusion in the early second trimester

Carbon Nanodot Additives Realize High‐Performance Air‐Stable p–i–n Perovskite Solar Cells Providing Efficiencies of up to 20.2

Syndromic and single gene disorders associated with fetal pleural effusion (I): Noonan syndrome, RASopathy and congenital lymphatic anomalies

Fetal trisomy 18 associated with congenital diaphragmatic hernia, choroid plexus cysts, clenched hands and a maternal origin of the extra chromosome 18

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

Recurrent neural tube defect and craniorachischisis detected in the first trimester and associated with maternal smoking

Prenatal diagnosis of distal 5p deletion syndrome associated with an abnormal first-trimester maternal serum screening result

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

Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations

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

Genetic testing using fetal urine at vesicocentesis in case of fetal megacystis

Chromosomal abnormalities associated with fetal pleural effusion (I): General overview

Molecular cytogenetic characterization of distal 5p deletion syndrome in a fetus with a de novo aberrant chromosome 5 at prenatal diagnosis

Detection of 45,X/46,X,r(X)(p11.3q22.1) in a 17-year-old girl with secondary amenorrhea, short stature and normal intelligence

Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly

Chromosomal abnormalities associated with fetal megacystis

Syndromic and single gene disorders associated with fetal megacystis (I): Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS)

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

Rapid diagnosis of maternal origin of fetal trisomy 13 by quantitative fluorescent polymerase chain reaction in a pregnancy associated with young maternal age and omphalocele on prenatal ultrasound

Mosaicism for trisomy 13 in a single colony at amniocentesis in a pregnancy associated with a favorable outcome

Craniorachischisis in a stillbirth associated with maternal smoking

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

Identification of a familial balanced chromosomal rearrangement in a couple presenting with recurrent pregnancy loss

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