Search Results - Liang-Kai Wang

Clinical and sonographic risk factors for developing pre-eclampsia refractory to aspirin prophylaxis by Chia-Chen Lee, Chie-Pein Chen, Chen-Yu Chen, Liang-Kai Wang, Yi-Yung Chen

Connect to this object online.

High-level mosaic trisomy 14 at amniocentesis in a pregnancy associated with congenital heart defects and intrauterine growth restriction on fetal ultrasound by Chih-Ping Chen, Fang-Tzu Wu, Liang-Kai Wang, Yen-Ting Pan, Meng-Shan Lee, Wayseen Wang

Connect to this object online.

Spontaneous rupture and massive hemoperitoneum from uterine leiomyomas and adenomyosis in a nongravid and unscarred uterus by Cheng-Ran Peng, Chie-Pein Chen, Kuo-Gon Wang, Liang-Kai Wang, Yi-Yung Chen, Chen-Yu Chen

Connect to this object online.

The reliability of transabdominal cervical length measurement in a low-risk obstetric population: Comparison with transvaginal measurement by Cheng-Ran Peng, Chie-Pein Chen, Kuo-Gon Wang, Liang-Kai Wang, Chen-Yu Chen, Yi-Yung Chen

Connect to this object online.

Changes in cervical elastography, cervical length and endocervical canal width after cerclage for cervical insufficiency: an observational ultrasound study by Meng-Hsuen Hsieh, Chie-Pein Chen, Fang-Ju Sun, Yi-Yung Chen, Liang-Kai Wang, Chen-Yu Chen

Connect to this object online.

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

Connect to this object online.

First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Yu-Ling Kuo, Yen-Ni Chen, Chen-Wen Pan, Wayseen Wang

Connect to this object online.

Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly,... by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Shin-Yin Huang, Wayseen Wang

Connect to this object online.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo deletion of 4q34.1→qter associated with low PAPP-A and low PlGF in the first-trimester maternal serum scr... by Chih-Ping Chen, Shin-Wen Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

Connect to this object online.

Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and con... by Chih-Ping Chen, Hoi-Kin Yip, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Wayseen Wang

Connect to this object online.

Late amniocentesis with uniparental disomy testing following successful in vitro fertilization and transfer of three mosaic embryos in a pregnancy with a favorable outcome by Chih-Ping Chen, Shyr-Yeu Lin, Chii-Ruey Tzeng, Liang-Kai Wang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Wayseen Wang

Connect to this object online.

Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Wayseen Wang

Connect to this object online.

High-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with positive NIPT for trisomy 21, prenatal progressive decrease of the trisomy 21 cell line, acute fatty li... by Chih-Ping Chen, Liang-Kai Wang, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang

Connect to this object online.

Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Kevin Ko, Yen-Ni Chen, Shin-Wen Chen, Meng-Shan Lee, Wayseen Wang

Connect to this object online.

Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3 by Shin-Wen Chen, Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Pei-Chen Wu, Yen-Ni Chen, Chen-Ju Lin, Wen-Ling Chen, Wayseen Wang

Connect to this object online.

22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, and congenital heart defects on prenatal ultrasound by Chih-Ping Chen, Tung-Yao Chang, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wen-Lin Chen, Wayseen Wang

Connect to this object online.

Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in... by Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

Connect to this object online.

Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Li-Feng Chen, Wayseen Wang

Connect to this object online.

Mosaic distal 10q deletion or 46,XY,del(10) (q26.13)/46,XY at amniocentesis and cordocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and... by Chih-Ping Chen, Liang-Kai Wang, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Chen-Chi Lee, Wen-Lin Chen, Chien-Ling Chiu, Wayseen Wang

Connect to this object online.

Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Wayseen Wang

Connect to this object online.