C. Pan

发表

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16.

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

3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Gene.

Short Communication Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysis

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012 .

A paternally derived inverted duplication of distal 14q with a terminal 14q deletion

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2005, American journal of medical genetics. Part A.

Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader-Willi syndrome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, 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.

Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, uinary tract anomalies, congenital heart defect and kyphoscoliosis

Chih-ping Chen, C. Pan, Chen‐Chi Lee, 1998, Prenatal diagnosis.

Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 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.

Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, American journal of medical genetics. Part A.

Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2013, Gene.

High-level mosaicism for 45,X in 45,X/46, XY at amniocentesis in a pregnancy with a favorable fetal outcome and cytogenetic discrepancy in various tissues.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Partial trisomy 10 (10q11.2→pter) and partial trisomy 18 (18p11.2→pter) associated with abnormal sonographic findings and a maternal serum screen‐positive result

C. Tzen, C. Pan, D. Town, 2004, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes.

Chih-ping Chen, S. Chern, C. Pan, 2012, Taiwanese journal of obstetrics & gynecology.

Balanced reciprocal translocations detected at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2013, Gene.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from inv dup(15).

Chih-ping Chen, S. Chern, Hsiang-Yu Lin, 2020, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2012, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome.

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

Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese Journal of Obstetrics & Gynecology.

REARRANGEMENTS INVOLVING CHROMOSOMES OTHER THAN CHROMOSOME 21

Chih-ping Chen, F. Tsai, S. Chern, 2009 .

Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of trisomy 8 mosaicism.

Chih-ping Chen, S. Chern, C. Pan, 2012, Taiwanese journal of obstetrics & gynecology.

Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3.

Chih-ping Chen, T. Ko, S. Chern, 2019, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11.

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

Prenatal diagnosis of pseudomosaicism for trisomy 20 at amniocentesis with a negative non-invasive prenatal testing (NIPT) result in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic 46,XX,dup(9)(q22.3q34.1)/46,XX at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Second‐trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature

Chih-ping Chen, C. Tzen, Sho-Jen Cheng, 2004, Prenatal diagnosis.

Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism.

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

Prenatal diagnosis of mosaic trisomy 16 by amniocentesis in a pregnancy associated with abnormal first-trimester screening result (low PAPP-A and low PlGF), intrauterine growth restriction and a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2021, Taiwanese journal of obstetrics & gynecology.

Unbalanced reciprocal translocations at amniocentesis.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling.

Chih-ping Chen, Ming-Chao Huang, F. Tsai, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 2q12.2→q13 encompassing MALL, NPHP1, RGPD6 and BUB1.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Late-onset fetal bilateral pleural effusions associated with Down syndrome.

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

A 12 Mb deletion of 6p24.1-->pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys.

Chih-ping Chen, C. Tzen, F. Tsai, 2009, European journal of medical genetics.

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 diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, T. Ko, S. Chern, 2017, 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.

Rapid Aneuploidy Diagnosis by Array Comparative Genomic Hybridization Using Uncultured Amniocytes in a Pregnancy With Fetal Nuchal Edema and Mild Ascites

Chih-ping Chen, C. Pan, Wayseen Wang, 2011 .

Prenatal diagnosis of the Dandy‐Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion

Chih-ping Chen, C. Tzen, Shuan-Pei Lin, 2002, Prenatal diagnosis.

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 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.

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese Journal of Obstetrics & Gynecology.

Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasi

Chih-ping Chen, S. Chern, C. Pan, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2014, Gene.

Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts

Chih-ping Chen, C. Tzen, S. Chern, 2001, Prenatal diagnosis.

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.

Chromosomal deletions detected at amniocentesis.

Chih-ping Chen, C. Pan, Wen‐Lin Chen, 2014, Taiwanese journal of obstetrics & gynecology.

Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2013, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism.

Chih-ping Chen, F. Tsai, S. Chern, 2009, Taiwanese journal of obstetrics & gynecology.

Partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31 →qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization.

Chih-ping Chen, F. Tsai, S. Chern, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 15q24 microdeletion.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial monosomy 1q (1q42.3-qter) associated with hydrocephalus and corpus callosum agenesis.

F. Tsai, S. Chern, C. Pan, 2010, Genetic counseling.

Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.

Chih-ping Chen, F. Tsai, S. Chern, 2011, Taiwanese journal of obstetrics & gynecology.

Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis.

Chih-ping Chen, T. Ko, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Higher male prevalence of chromosomal mosaicism detected by amniocentesis.

Chih-ping Chen, Shin-Wen Chen, C. Pan, 2018, 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.

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2022, Taiwanese journal of obstetrics & gynecology.

Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.

Chih-ping Chen, S. Chern, C. Pan, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q.

F. Tsai, C. Pan, C. Chen, 2010, Genetic counseling.

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome.

Chih-ping Chen, S. Chern, C. Pan, 2023, Taiwanese journal of obstetrics & gynecology.

Molecular cytogenetic characterization of del(X)(p22.33)mat and de novo dup(4)(q34.3q35.2) in a male fetus with multiple anomalies of facial dysmorphism, ventriculomegaly, congenital heart defects, short long bones and clinodactyly.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2023, Taiwanese journal of obstetrics & gynecology.

A 5.3-Mb duplication of 9p12 --> p13.1 characterized by array CGH in a female infant with developmental delay.

F. Tsai, S. Chern, C. Pan, 2010, Genetic counseling.

Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2023, Taiwanese journal of obstetrics & gynecology.