Search Results - Shin-Wen Chen

Spontaneous resolution of septated cystic hygroma with a severely increased nuchal translucency thickness of 5.8 mm detected in the first-trimester in a pregnancy with no abnormali... by Chih-Ping Chen, Shin-Wen Chen, Fang-Tzu Wu, Yen-Ting Pan, Wayseen Wang

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A false-positive result at non-invasive prenatal testing due to maternal 17p12 microduplication by Chih-Ping Chen, Shin-Wen Chen, Peih-Shan Wu, Fang-Tzu Wu, Wayseen Wang

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The significance of karyotyping and azoospermia factor analysis in patients with nonobstructive azoospermia or oligozoospermia by Shin-Wen Chen, Chih-Ping Chen, Schu-Rern Chern, Yu-Ling Kuo, Chien-Ling Chiu

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Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum by Chih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang

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Prenatal diagnosis of familial 2p15 microduplication associated with pulmonary artery stenosis, single umbilical artery and left foot postaxial polydactyly on fetal ultrasound by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Prenatal diagnosis of persistent left superior vena cava, polyhydramnios and a small gastric bubble in a fetus with VACTERL association by Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Shin-Wen Chen, Dai-Dyi Town, Wayseen Wang

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Prenatal diagnosis and management of monozygotic twins discordant for severe fetal abnormalities by Chih-Ping Chen, Steven W. Shaw, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a twin pregnancy with a favorable outcome by Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Wen Pan, Wayseen Wang

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Molecular cytogenetic characterization of a de novo chromosome 1q41-q42.11 microdeletion of paternal origin in a 15-year-old boy with mental retardation, developmental delay, autis... by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analys... by Chih-Ping Chen, Shih-Shien Weng, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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45,X/46,XX at amniocentesis associated with a favorable outcome and postnatal decrease of the 45,X cell line by Chih-Ping Chen, Shin-Wen Chen, Chi-Kang Lin, Fang-Tzu Wu, Yun-Yi Chen, Li-Feng Chen, Wayseen Wang

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Prenatal diagnosis of mosaicism for trisomy 17 in a single colony at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outco... by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Wen Pan, Wayseen Wang

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Prenatal diagnosis of familial 22q11.2 deletion syndrome in a pregnancy with concomitant cardiac and urinary tract abnormalities in the fetus and the mother by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Detection of paternal origin of fetal trisomy 18 in a pregnancy conceived by assisted reproductive technology and in vitro fertilization by Chih-Ping Chen, Schu-Rern Chern, Liang-Kai Wang, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang

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Application of array comparative genomic hybridization analysis for rapid differential diagnosis of a chromosome euchromatic variant of dup 22q13.3 at amniocentesis by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Wayseen Wang

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Prenatal diagnosis of a 1.651-Mb 19q13.42-q13.43 microdeletion in a fetus with micrognathia and bilateral pyelectasis on prenatal ultrasound by Chih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

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Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and l... by Chih-Ping Chen, Shuan-Pei Lin, Yu-Peng Liu, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Wayseen Wang

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Detection of paternal origin of fetal trisomy 21 in a pregnancy with isolated ventriculomegaly but without advanced parental age by Chih-Ping Chen, Wan-Chun Huang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Wayseen Wang

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Prenatal diagnosis of trisomy 11 in a single colony of cultured amniocytes at amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Cheng-En Hsieh, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang

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Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome by Chih-Ping Chen, Chen-Yu Chen, Tung-Yao Chang, Hsiu-Yu Yang, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang

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