Search Results - Yen-Ni Chen

Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result by Chih-Ping Chen, Shuan-Pei Lin, Hui-Bo Li, Yen-Ni Chen, Wayseen Wang

Connect to this object online.

Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report by Yi-Ying Li, Ksenia Olisova, Yen-Ni Chen, Chia-Hsieh Chang, Tung-Yao Chang

Connect to this object online.

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

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.

Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling by Chih-Ping Chen, Schu-Rern Chern, Nan-Chang Chiu, Yu-Peng Liu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang

Connect to this object online.

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review by Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Peih-Shan Wu, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang

Connect to this object online.

Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality by Chih-Ping Chen, Chung-Hu Fu, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang

Connect to this object online.

Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome by Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang

Connect to this object online.

Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, a... by Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang

Connect to this object online.

Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus cal... by Chih-Ping Chen, Cheng-Ran Peng, Tung-Yao Chang, Wan-Yuo Guo, Yen-Ni Chen, Peih-Shan Wu, Dai-Dyi Town, Wayseen Wang

Connect to this object online.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter) by Chih-Ping Chen, Fung-Yu Hung, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang

Connect to this object online.

Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder by Chih-Ping Chen, Shuan-Pei Lin, Chung-Lin Lee, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, 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.

Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature by Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Yu-Ling Kuo, Yen-Ni Chen, Peih-Shan Wu, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang

Connect to this object online.

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with s... by Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Meng-Shan Lee, 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 and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Corn... by Chih-Ping Chen, Ming-Huei Lin, Yi-Yung Chen, Schu-Rern Chern, Yen-Ni Chen, Peih-Shan Wu, Chen-Wen Pan, Meng-Shan Lee, Wayseen Wang

Connect to this object online.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome by Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang

Connect to this object online.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallo... by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

Connect to this object online.