Y. Chen

发表

Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result.

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion.

Chih-ping Chen, T. Ko, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

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.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2017, Taiwanese journal of obstetrics & gynecology.

Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature.

Chih-ping Chen, Ming-Chao Huang, S. Chern, 2015, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes.

Chih-ping Chen, Yeou-Lih Wang, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal Ultrasound Findings of Pregnancy Associated with Zika Virus Infection

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2016 .

Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome.

Chih-ping Chen, Shin-Wen Chen, Wayseen Wang, 2016, Taiwanese journal of obstetrics & gynecology.

Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Reply to Comment on An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2018, Journal of medical ultrasound.

An Intrauterine Gestational sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2017, Journal of medical ultrasound.

An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2017, Journal of medical ultrasound.

Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2017, Taiwanese journal of obstetrics & gynecology.

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 Fallot.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism.

Chih-ping Chen, S. Chern, C. Pan, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal Ultrasound Evaluation and Outcome of Pregnancy with Fetal Cystic Hygromas and Lymphangiomas

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2017, Journal of medical ultrasound.

Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly.

Chih-ping Chen, Wan-Yuo Guo, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction.

Chih-ping Chen, T. Ko, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2017, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion.

Chih-ping Chen, T. Ko, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2015, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2017, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2016, Taiwanese journal of obstetrics & gynecology.

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 short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese journal of obstetrics & gynecology.

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.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2017, Taiwanese Journal of Obstetrics & Gynecology.

Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2018, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome.

Chih-ping Chen, T. Ko, S. Chern, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis.

Chih-ping Chen, Shing-Jyh Chang, S. Chern, 2016, Taiwanese Journal of Obstetrics & Gynecology.

22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, and congenital heart defects on prenatal ultrasound.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.

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.

Chih-ping Chen, N. Chiu, S. Chern, 2016, Taiwanese Journal of Obstetrics & Gynecology.

Reply to Comment on An Intrauterine Gestational Sac Surrounded by Thin Myometrium at Fundus

Chih-ping Chen, Shin-Wen Chen, Chen‐Ju Lin, 2018, Journal of medical ultrasound.

Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2016, Taiwanese journal of obstetrics & gynecology.