Yu-Ting Chen, Ph.D. - Publications

Affiliations: 
2006 University of Illinois, Urbana-Champaign, Urbana-Champaign, IL 
Area:
Curriculum and Instruction Education, Folklore, Art Education

61 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Chen YT, Wang W, Li L, Kelly R, Xie G. Obstacle effects on electrocommunication with applications to object detection of underwater robots. Bioinspiration & Biomimetics. PMID 31318703 DOI: 10.1088/1748-3190/ab336c  0.32
2014 Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, Wu PS, Chen YT, Chang SY. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Taiwanese Journal of Obstetrics & Gynecology. 53: 248-51. PMID 25017279 DOI: 10.1016/j.tjog.2014.04.021  0.32
2014 Guo XJ, Tian XS, Ruan Z, Chen YT, Wu L, Gong Q, Wang W, Zhang HY. Dysregulation of neurotrophic and inflammatory systems accompanied by decreased CREB signaling in ischemic rat retina. Experimental Eye Research. 125: 156-63. PMID 24954538 DOI: 10.1016/j.exer.2014.06.003  0.32
2014 Chen CP, Lin CL, Ko TM, Chern SR, Chen YT, Wu PS, Kuo YL, Lee MS, Wang W. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p. Taiwanese Journal of Obstetrics & Gynecology. 53: 126-8. PMID 24767666 DOI: 10.1016/j.tjog.2013.11.003  0.32
2014 Chen CP, Lin MH, Chern SR, Chen YT, Wu PS, Kuo YL, Lee MS, Wang W. Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization. Taiwanese Journal of Obstetrics & Gynecology. 53: 123-5. PMID 24767665 DOI: 10.1016/j.tjog.2013.11.002  0.32
2014 Chen CP, Wang PT, Lin SP, Chern SR, Chen YT, Wu PS, Kuo YL, Chen WL, Wang W. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes. Taiwanese Journal of Obstetrics & Gynecology. 53: 120-2. PMID 24767664 DOI: 10.1016/j.tjog.2013.11.001  0.32
2014 Chen CP, Wang LK, Chern SR, Wu PS, Chen YT, Kuo YL, Chen WL, Lee MS, Wang W. Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization, and literature review. Taiwanese Journal of Obstetrics & Gynecology. 53: 79-85. PMID 24767652 DOI: 10.1016/j.tjog.2013.12.002  0.32
2014 Chen CP, Su YN, Lin MH, Wang TY, Chern SR, Kuo YL, Chen YT, Wang W. Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia. Taiwanese Journal of Obstetrics & Gynecology. 53: 68-73. PMID 24767650 DOI: 10.1016/j.tjog.2013.10.036  0.32
2014 Chen CP, Lin SP, Chern SR, Kuo YL, Wu PS, Chen YT, Lee MS, Wang W. Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation. Gene. 535: 88-92. PMID 24279999 DOI: 10.1016/j.gene.2013.11.026  0.32
2013 Chen CP, Chang SD, Lee YX, Shih JC, Chern SR, Wu PS, Su JW, Chen YT, Hsieh AH, Chen TH, Chen LF, Wang W. WITHDRAWN: Corrigendum to "Ring chromosome 21 presenting with sacrococcygeal teratoma: Prenatal diagnosis, molecular cytogenetic characterization and literature review" [Gene 522 (2013) 111-116]. Gene. PMID 24412089 DOI: 10.1016/j.gene.2013.06.020  0.32
2013 Chen CP, Chang SD, Wang TH, Wang LK, Tsai JD, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Wang W. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family. Taiwanese Journal of Obstetrics & Gynecology. 52: 551-7. PMID 24411042 DOI: 10.1016/j.tjog.2013.10.017  0.32
2013 Chen CP, Chang SD, Su JW, Chen YT, Wang W. Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth. Taiwanese Journal of Obstetrics & Gynecology. 52: 454-6. PMID 24075395 DOI: 10.1016/j.tjog.2013.06.008  0.32
2013 Chen CP, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Pan CW, Wang W. 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. Taiwanese Journal of Obstetrics & Gynecology. 52: 450-3. PMID 24075394 DOI: 10.1016/j.tjog.2013.06.007  0.32
2013 Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism. Taiwanese Journal of Obstetrics & Gynecology. 52: 395-400. PMID 24075380 DOI: 10.1016/j.tjog.2013.06.004  0.32
2013 Chen CP, Chang TY, Guo WY, Wu PC, Wang LK, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W. Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review. Gene. 532: 152-9. PMID 24055730 DOI: 10.1016/j.gene.2013.09.044  0.32
2013 Chen CP, Huang MC, Chen YY, Chern SR, Wu PS, Chen YT, Su JW, Wang W. Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect. Gene. 531: 496-501. PMID 24036431 DOI: 10.1016/j.gene.2013.09.010  0.32
2013 Chen CP, Lee MJ, Chern SR, Wu PS, Su JW, Chen YT, Lee MS, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14). Gene. 529: 351-6. PMID 23948085 DOI: 10.1016/j.gene.2013.07.063  0.32
2013 Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13. Gene. 529: 163-8. PMID 23933417 DOI: 10.1016/j.gene.2013.07.050  0.32
2013 Chen CP, Lin SP, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Wang W. An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy. Gene. 529: 176-80. PMID 23933416 DOI: 10.1016/j.gene.2013.07.045  0.32
2013 Chen CP, Chen M, Su YN, Huang JP, Chern SR, Wu PS, Su JW, Chang SP, Chen YT, Lee CC, Chen LF, Pan CW, Wang W. Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review. Gene. 529: 169-75. PMID 23933412 DOI: 10.1016/j.gene.2013.07.048  0.32
2013 Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen WL, Wang W. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review. Gene. 527: 405-9. PMID 23791650 DOI: 10.1016/j.gene.2013.06.009  0.32
2013 Chen CP, Lin SP, Liu YP, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Wang W. 6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay. Gene. 523: 99-102. PMID 23578800 DOI: 10.1016/j.gene.2013.03.121  0.32
2013 Chen CP, Ko TM, Su YN, Su JW, Chen YT, Lee CC, Chen LF, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21). Taiwanese Journal of Obstetrics & Gynecology. 52: 147-51. PMID 23548242 DOI: 10.1016/j.tjog.2012.09.037  0.32
2013 Chen CP, Chang SD, Chueh HY, Su YN, Chern SR, Su JW, Chen YT, Chen WL, Lee MS, Wang W. Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20. Taiwanese Journal of Obstetrics & Gynecology. 52: 145-6. PMID 23548241 DOI: 10.1016/j.tjog.2013.01.021  0.32
2013 Chen CP, Hwang KS, Su HY, Lin SP, Su YN, Chern SR, Su JW, Chen YT, Chen WL, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry. Taiwanese Journal of Obstetrics & Gynecology. 52: 125-8. PMID 23548233 DOI: 10.1016/j.tjog.2012.08.002  0.32
2013 Chen CP, Su YN, Lin SP, Chern SR, Su JW, Chen YT, Lee MS, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry. Taiwanese Journal of Obstetrics & Gynecology. 52: 120-4. PMID 23548232 DOI: 10.1016/j.tjog.2013.01.015  0.32
2013 Chen CP, Su YN, Su JW, Chern SR, Chen YT, Chen LF, Wang W. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis. Taiwanese Journal of Obstetrics & Gynecology. 52: 97-105. PMID 23548227 DOI: 10.1016/j.tjog.2013.01.012  0.32
2013 Chen CP, Cheng PJ, Chang SD, Lee YX, Shih JC, Chern SR, Wu PS, Su JW, Chen YT, Hsieh AH, Chen TH, Chen LF, Wang W. Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review. Gene. 522: 111-6. PMID 23545316 DOI: 10.1016/j.gene.2013.03.064  0.32
2013 Chen CP, Chang SJ, Chern SR, Wu PS, Chen YT, Su JW, Chen WL, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1). Gene. 521: 311-5. PMID 23545313 DOI: 10.1016/j.gene.2013.03.100  0.32
2013 Chen CP, Lin CJ, Chang TY, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Chen LF, Wang W. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization. Gene. 519: 164-8. PMID 23403238 DOI: 10.1016/j.gene.2013.01.055  0.32
2013 Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W. 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. Gene. 516: 138-42. PMID 23266815 DOI: 10.1016/j.gene.2012.12.051  0.32
2012 Chen CP, Su YN, Chern SR, Chen YT, Su JW, Pan CW, Wang W. Prenatal diagnosis of trisomy 8 mosaicism. Taiwanese Journal of Obstetrics & Gynecology. 51: 666-8. PMID 23276580 DOI: 10.1016/j.tjog.2012.09.030  0.32
2012 Chen CP, Chang SD, Chen YT, Su JW, Town DD, Wang W. Mosaic isochromosome 20q detected at amniocentesis: a likely cell culture artifact. Taiwanese Journal of Obstetrics & Gynecology. 51: 663-5. PMID 23276579 DOI: 10.1016/j.tjog.2012.09.029  0.32
2012 Chen CP, Ko TM, Su YN, Chern SR, Su JW, Chen YT, Town DD, Wang W. Prenatal diagnosis of mosaic tetrasomy 18p. Taiwanese Journal of Obstetrics & Gynecology. 51: 625-9. PMID 23276569 DOI: 10.1016/j.tjog.2012.09.020  0.32
2012 Chen CP, Su YN, Chern SR, Chen YT, Wu PS, Su JW, Pan CW, Wang W. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis. Taiwanese Journal of Obstetrics & Gynecology. 51: 603-11. PMID 23276565 DOI: 10.1016/j.tjog.2012.09.016  0.32
2012 Chen CP, Su YN, Chern SR, Su JW, Chen YT, Lee CC, Wang W. Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation Taiwanese Journal of Obstetrics and Gynecology. 51: 485-488. PMID 23040947 DOI: 10.1016/j.tjog.2012.07.037  0.32
2012 Chen CP, Chang SD, Chueh HY, Su YN, Su JW, Chern SR, Chen YT, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W. Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes. Taiwanese Journal of Obstetrics & Gynecology. 51: 475-80. PMID 23040945 DOI: 10.1016/j.tjog.2012.07.035  0.32
2012 Chen CP, Su YN, Chen YY, Chern SR, Su JW, Chen YT, Town DD, Wang W. Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly Taiwanese Journal of Obstetrics and Gynecology. 51: 471-474. PMID 23040944 DOI: 10.1016/j.tjog.2012.07.034  0.32
2012 Chen CP, Chen M, Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hwa-Ruey Hsieh A, Hwa-Jiun Hsieh A, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2. Taiwanese Journal of Obstetrics & Gynecology. 51: 411-7. PMID 23040927 DOI: 10.1016/j.tjog.2012.07.017  0.32
2012 Chen CP, Chang SD, Su YN, Chen M, Chern SR, Su JW, Chen YT, Chen WL, Pan CW, Lee MS, Wang W. 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 pyelectasis. Taiwanese Journal of Obstetrics & Gynecology. 51: 405-10. PMID 23040926 DOI: 10.1016/j.tjog.2012.07.016  0.32
2012 Chen CP, Chen M, Su YN, Huang JP, Ma GC, Chang SP, Chern SR, Chen YT, Su JW, Lee CC, Town DD, Wang W. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. Taiwanese Journal of Obstetrics & Gynecology. 51: 245-52. PMID 22795102 DOI: 10.1016/j.tjog.2012.04.015  0.32
2012 Chen CP, Su YN, Chen M, Tsai FJ, Chen YY, Ma GC, Chang SP, Su JW, Chen YT, Chen WL, Chen LF, Wang W. 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. Taiwanese Journal of Obstetrics & Gynecology. 51: 134-8. PMID 22482988 DOI: 10.1016/j.tjog.2012.01.030  0.32
2012 Chen CP, Huang HK, Su YN, Chern SR, Su JW, Lee CC, Town DD, Chen WL, Chen YT, Wang W. Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism. Taiwanese Journal of Obstetrics & Gynecology. 51: 77-82. PMID 22482973 DOI: 10.1016/j.tjog.2012.01.015  0.32
2012 Chen CP, Lin YH, Chou SY, Su YN, Chern SR, Chen YT, Town DD, Chen WL, Wang W. Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3. Taiwanese Journal of Obstetrics & Gynecology. 51: 71-6. PMID 22482972 DOI: 10.1016/j.tjog.2012.01.014  0.32
2011 Chen CP, Hung FY, Su YN, Chern SR, Su JW, Lee CC, Chen YT, Chen WL, Wang W. Prenatal diagnosis of mosaic trisomy 9. Taiwanese Journal of Obstetrics & Gynecology. 50: 549-53. PMID 22212338 DOI: 10.1016/j.tjog.2011.10.031  0.32
2011 Chen CP, Su YN, Chen YY, Su JW, Chern SR, Chen YT, Chen WL, Chen LF, Wang W. 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. Taiwanese Journal of Obstetrics & Gynecology. 50: 506-11. PMID 22212326 DOI: 10.1016/j.tjog.2011.10.019  0.32
2011 Chen CP, Huang HK, Ling PY, Su YN, Chen M, Tsai FJ, Wu PC, Chern SR, Chen YT, Lee CC, Wang W. A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings. Taiwanese Journal of Obstetrics & Gynecology. 50: 492-8. PMID 22212323 DOI: 10.1016/j.tjog.2011.10.016  0.32
2011 Chen CP, Su YN, Hsu CY, Chern SR, Lee CC, Chen YT, Chen WL, Wang W. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy. Taiwanese Journal of Obstetrics & Gynecology. 50: 485-91. PMID 22212322 DOI: 10.1016/j.tjog.2011.10.015  0.32
2011 Chen CP, Su YN, Chen YT, Chen WL, Hsu LJ, Wang W. Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene. Taiwanese Journal of Obstetrics & Gynecology. 50: 401-4. PMID 22030066 DOI: 10.1016/j.tjog.2011.06.002  0.32
2011 Chen CP, Su YN, Lin SY, Chern SR, Chen YT, Lee MS, Wang W. Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction. Taiwanese Journal of Obstetrics & Gynecology. 50: 390-3. PMID 22030063 DOI: 10.1016/j.tjog.2011.07.011  0.32
2011 Chen CP, Lin YH, Au HK, Su YN, Hsu CY, Liu YP, Wu PC, Chern SR, Chen YT, Chen LF, Hsieh AH, Wang W. Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3). Taiwanese Journal of Obstetrics & Gynecology. 50: 359-65. PMID 22030053 DOI: 10.1016/j.tjog.2011.07.004  0.32
2011 Chen CP, Su YN, Chen YY, Chern SR, Liu YP, Wu PC, Lee CC, Chen YT, Wang W. Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction. Taiwanese Journal of Obstetrics & Gynecology. 50: 345-52. PMID 22030051 DOI: 10.1016/j.tjog.2011.07.014  0.32
2011 Chen CP, Su YN, Lin HH, Chern SR, Tsai FJ, Wu PC, Lee CC, Chen YT, Wang W. De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure. Taiwanese Journal of Obstetrics & Gynecology. 50: 339-44. PMID 22030050 DOI: 10.1016/j.tjog.2011.01.018  0.32
2011 Chen CP, Chen M, Pan YJ, Su YN, Chern SR, Tsai FJ, Chen YT, Wang W. Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review. Taiwanese Journal of Obstetrics & Gynecology. 50: 331-8. PMID 22030049 DOI: 10.1016/j.tjog.2011.07.013  0.32
2011 Chen CP, Liou JD, Chiang CH, Su YN, Chern SR, Tsai FJ, Wu PC, Chen YT, Lee CC, Chen WL, Wang W. Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis. Taiwanese Journal of Obstetrics & Gynecology. 50: 245-8. PMID 21791321 DOI: 10.1016/j.tjog.2011.04.006  0.32
2011 Chen CP, Kuo YK, Su YN, Chern SR, Tsai FJ, Wu PC, Chen YT, Town DD, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly. Taiwanese Journal of Obstetrics & Gynecology. 50: 182-7. PMID 21791305 DOI: 10.1016/j.tjog.2011.04.001  0.32
2011 Chen CP, Su YN, Chern SR, Hsu CY, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Wang W. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwanese Journal of Obstetrics & Gynecology. 50: 67-73. PMID 21482378 DOI: 10.1016/j.tjog.2011.01.038  0.32
2010 Chen CP, Lin CC, Ko TM, Tsai FJ, Chern SR, Lee CC, Chen YT, Wu PC, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21. Taiwanese Journal of Obstetrics & Gynecology. 49: 377-80. PMID 21056330 DOI: 10.1016/S1028-4559(10)60080-0  0.32
2010 Chen CP, Su YN, Chern SR, Hwu YM, Lin SP, Hsu CH, Tsai FJ, Wang TY, Wu PC, Lee CC, Chen YT, Chen LF, Wang W. Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses. Taiwanese Journal of Obstetrics & Gynecology. 49: 333-40. PMID 21056320 DOI: 10.1016/S1028-4559(10)60070-8  0.32
2010 Chen CP, Kuo YT, Lin SP, Su YN, Chen YJ, Hsueh RY, Lin YH, Wu PC, Lee CC, Chen YT, Wang W. Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. Taiwanese Journal of Obstetrics & Gynecology. 49: 327-32. PMID 21056319 DOI: 10.1016/S1028-4559(10)60069-1  0.32
2010 Chen CP, Lin SP, Chern SR, Tsai FJ, Wu PC, Lee CC, Chen YT, Chen WL, Wang W. A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings. European Journal of Medical Genetics. 53: 329-32. PMID 20541044 DOI: 10.1016/j.ejmg.2010.06.004  0.32
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