Li‐Feng Chen

发表

Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.

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

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.

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 of de novo pure partial monosomy 4p (4p15.1 → pter) in a growth‐restricted fetus with a Greek warrior helmet face and unilateral facial cleft on three‐dimensional ultrasound

Chih-ping Chen, Wayseen Wang, Wen‐Lin Chen, 2004, Prenatal diagnosis.

Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects.

Chih-ping Chen, Jian-Pei Huang, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial monosomy 2q (2q37.3→qter) and partial trisomy 10q (10q24.31→qter) of paternal origin associated with increased nuchal translucency and abnormal maternal serum screening results.

Chih-ping Chen, K. Seow, S. Chern, 2020, Taiwanese journal of obstetrics & gynecology.

Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).

Chih-ping Chen, S. Chern, H. Au, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus.

Chih-ping Chen, T. Ko, S. Chern, 2021, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound.

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

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold.

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

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis.

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

Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.

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

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 and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome.

Chih-ping Chen, Wayseen Wang, Yi-Yung Chen, 2011, 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 diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review.

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

Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9 p deletion and literature review

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

High-level mosaicism for 45,X in 45,X/46,X,idic(Y)(q11.2) at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & gynecology.

Perinatal cytogenetic discrepancy in a pregnancy with mosaic 45,X/46, XY at amniocentesis and a favorable outcome.

Chih-ping Chen, S. Chern, Shin-Wen Chen, 2022, Taiwanese journal of obstetrics & 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.

Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.

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

Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review.

Wan-Yuo Guo, Li-Feng Chen, Chih-ping Chen, 2013, Gene.

Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2010, Taiwanese journal of obstetrics & gynecology.

Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review.

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

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 of low‐level mosaic trisomy 7 by amniocentesis

Chih-ping Chen, S. Chern, Wayseen Wang, 2005, Prenatal diagnosis.

Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly.

Chih-ping Chen, S. Chern, Wayseen Wang, 2011, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism.

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

Prenatal diagnosis of congenital chylothorax associated with de novopartial trisomy 12q (12q21.2→qter)

Chih-ping Chen, C. Tzen, S. Chern, 2006, Prenatal diagnosis.

Wolf-Hirschhorn syndrome: Prenatal diagnosis and molecular cytogenetic characterization of a de novo distal deletion of 4p (4p16.1 → pter) in a fetus with facial cleft and preaxial polydactyly.

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

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.

Chih-ping Chen, F. Tsai, T. Ko, 2010, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22.

Chih-ping Chen, F. Tsai, S. Chern, 2010, 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 de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus

Chih-ping Chen, S. Chern, Ming-Hong Chen, 1998, Prenatal diagnosis.

Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome.

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

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction

Chih-ping Chen, C. Tzen, S. Chern, 2003, Prenatal diagnosis.

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.

Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency

Chih-ping Chen, S. Chern, Wayseen Wang, 2005, Prenatal diagnosis.

Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis.

Chih-ping Chen, S. Chern, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses.

Chih-ping Chen, F. Tsai, S. Chern, 2010, 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 a proximal deletion of 22q (22q11.2→q11.21).

Chih-ping Chen, T. Ko, Wayseen Wang, 2013, Taiwanese journal of obstetrics & gynecology.

Unbalanced reciprocal translocations at amniocentesis.

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

Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion

Chih-ping Chen, C. Tzen, S. Chern, 2003, Prenatal diagnosis.

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.

Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.

Chih-ping Chen, F. Tsai, Shuan-Pei Lin, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of a fetus with distal 10q trisomy

Chih-ping Chen, Wayseen Wang, Tao‐Yeuan Wang, 1999, Prenatal diagnosis.

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.

Prenatal diagnosis of low‐level mosaicism for a small XIST‐negative supernumerary ring X chromosome in a nondysmorphic male fetus

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2006, Prenatal diagnosis.

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.

Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome.

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

Perinatal findings of partial trisomy 13q (13q14.1→qter) resulting from paternal pericentric inversion of chromosome 13

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2005, Prenatal diagnosis.

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.

Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects.

Chih-ping Chen, S. Chern, Peih-Shan Wu, 2019, Taiwanese journal of obstetrics & gynecology.

Detection of mosaic balanced homologous acrocentric rearrangement rea(21q21q) in a woman with repeated pregnancy losses.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2012, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis of partial monosomy 18p(18p11.2→pter) and trisomy 21q(21q22.3→qter) with alobar holoprosencephaly and premaxillary agenesis

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

Prenatal diagnosis of mosaic ring chromosome 4

Chih-ping Chen, C. Tzen, Wayseen Wang, 2007, Prenatal diagnosis.

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.

Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization.

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 ring chromosome 2.

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

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.

Chih-ping Chen, F. Tsai, S. Chern, 2010, 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 of pure distal 18q deletion

Chih-ping Chen, C. Tzen, S. Chern, 2006, Prenatal diagnosis.

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.

Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism.

Chih-ping Chen, F. Tsai, Wayseen Wang, 2012, 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.

Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis.

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

Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints.

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

Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin.

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

Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones

Chih-ping Chen, S. Chern, Chen‐Chi Lee, 1998, Prenatal diagnosis.

Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy‐Walker variant and trigonocephaly

Chih-ping Chen, C. Tzen, Wayseen Wang, 2002, Prenatal diagnosis.

Prenatal diagnosis of the distal 11q deletion and review of the literature

Chih-ping Chen, C. Tzen, S. Chern, 2004, Prenatal diagnosis.

Rapid Diagnosis of Trisomy 21 by Array Comparative Genomic Hybridization using Uncultured Amniocytes in a Pregnancy with Isolated Ventriculomegaly in the Fetus

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

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 and genetic analysis of X chromosome polysomy 49,XXXXY

Chih-Long Chang, Chih-ping Chen, S. Chern, 2000, Prenatal diagnosis.

Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18

Chih-ping Chen, S. Chern, Wayseen Wang, 2000, Prenatal diagnosis.

A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow joints.

Chih-ping Chen, S. Chern, Shuan-Pei Lin, 2018, Taiwanese journal of obstetrics & gynecology.

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 a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.

Chih-ping Chen, T. Ko, S. Chern, 2021, Taiwanese journal of obstetrics & gynecology.

Postnatal identi fi cation of high plasma renin activity or hypercalcemia might aid in the diagnosis

Chih-ping Chen, Wayseen Wang, Wen‐Lin Chen, 2004 .

Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→ter→qter)

Chih-ping Chen, Wayseen Wang, Tung-Yao Chang, 2006, Prenatal diagnosis.

Second‐trimester sonographic demonstration of retrognathia and bilateral pyelectasis in a fetus with a duplication of chromosome 10q24.1→qter

Chih-ping Chen, C. Tzen, Wayseen Wang, 2003, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

of partial trisomy

Chih-ping Chen, Shuan-Pei Lin, Wayseen Wang, 2022 .

Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes.

Chih-ping Chen, T. Ko, S. Chern, 2021, Taiwanese journal of obstetrics & gynecology.