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Chen-Chi Lee

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Physiology

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Chromosomes, Human, Pair 18

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Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Chen-Ju Lin; Jun-Wei Su; Tung-Yao Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Jun-Wei Su; Tsung-Hsien Su; Wayseen Wang
Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother.
Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Hsu-Kuang Huang; Chen-Chi Lee; Pei-Ying Ling; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.

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All Publications

2013: Chih-Ping Chen; Li-Feng Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Chen-Ju Lin; Jun-Wei Su; Tung-Yao Chang; Peih-Shan Wu; Wayseen Wang
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization.
Gene 2013;519(1):164-8.
2012: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Jun-Wei Su; Tsung-Hsien Su; Wayseen Wang
Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother.
Taiwanese journal of obstetrics & gynecology 2012;51(4):630-4.
2011: Chih-Ping Chen; Ming Chen; Yu-Ting Chen; Schu-Rern Chern; Hsu-Kuang Huang; Chen-Chi Lee; Pei-Ying Ling; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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 2011;50(4):492-8.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Chin-Yuan Hsu; Chen-Chi Lee; Yi-Ning Su; Wayseen Wang
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 2011;50(4):485-91.
2011: Chih-Ping Chen; Yu-Ting Chen; Yi-Yung Chen; Schu-Rern Chern; Chen-Chi Lee; Yu-Peng Liu; Yi-Ning Su; Pei-Chen Wu; Wayseen Wang
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 2011;50(3):345-52.
2011: Chih-Ping Chen; Yu-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Hung-Hung Lin; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
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 2011;50(3):339-44.
2011: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p.
Taiwanese journal of obstetrics & gynecology 2011;50(2):249-52.
2011: Chih-Ping Chen; Wen-Lin Chen; Yu-Ting Chen; Schu-Rern Chern; Chi-Hsin Chiang; Chen-Chi Lee; Jui-Der Liou; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2011;50(2):245-8.
2011: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Ming-Huei Lin; Chen-Wen Pan; Yi-Ning Su; Fuu-Jen Tsai; Pei-Chen Wu; Wayseen Wang
Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
Taiwanese journal of obstetrics & gynecology 2011;50(2):205-11.
2011: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Chin-Yuan Hsu; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Wayseen Wang
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 2011;50(1):67-73.
2011: Chih-Ping Chen; Pei-Chen Wu; Chen-Ju Lin; Schu-Rern Chern; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Unbalanced reciprocal translocations at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2011;50(1):48-57.
2011: Chih-Ping Chen; M Chen; Yann-Jang Chen; Schu-Rern Chern; Chen-Chi Lee; Shuan-Pei Lin; Y P Liu; Y N Su; Fuu-Jen Tsai; T Y Wang; Wayseen Wang
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses.
Genetic counseling (Geneva, Switzerland) 2011;22(3):273-80.
2010: Chih-Ping Chen; Ming Chen; Tsang-Ming Ko; Gwo-Chin Ma; Fuu-Jen Tsai; Ming-Song Tsai; Pei-Chen Wu; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
Taiwanese journal of obstetrics & gynecology 2010;49(4):500-5.
2010: Chih-Ping Chen; Ming Chen; Yi-Ning Su; Chin-Yuan Hsu; Fuu-Jen Tsai; Schu-Rern Chern; Pei-Chen Wu; Chen-Chi Lee; Wayseen Wang
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Taiwanese journal of obstetrics & gynecology 2010;49(4):473-80.
2010: Chih-Ping Chen; Hsien-Ming Lin; Yi-Ning Su; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Taiwanese journal of obstetrics & gynecology 2010;49(3):341-50.
2010: Chih-Ping Chen; Yi-Ning Su; Schu-Rern Chern; Yuh-Ming Hwu; Shuan-Pei Lin; Chyong-Hsin Hsu; Fuu-Jen Tsai; Tao-Yeuan Wang; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Li-Feng Chen; Wayseen Wang
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Taiwanese journal of obstetrics & gynecology 2010;49(3):333-40.
2010: Chih-Ping Chen; Yung-Ting Kuo; Shuan-Pei Lin; Yi-Ning Su; Yann-Jang Chen; Rui-Yuan Hsueh; Yi-Hui Lin; Pei-Chen Wu; Chen-Chi Lee; Yu-Ting Chen; Wayseen Wang
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 2010;49(3):327-32.
2010: Chih-Ping Chen; Chyi-Chyang Lin; Yi-Ning Su; Fuu-Jen Tsai; Ju-Ting Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Li-Feng Chen; Pei-Chen Wu; Wayseen Wang
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.
Taiwanese journal of obstetrics & gynecology 2010;49(2):188-91.
2010: Chih-Ping Chen; Schu-Rern Chern; Pei-Chen Wu; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Unbalanced and balanced heterologous acrocentric rearrangements involving chromosome 21 at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2010;49(1):62-8.
2009: Chih-Ping Chen; Schu-Rern Chern; Fuu-Jen Tsai; Pei-Chen Wu; Shu-Shien Chiang; Chen-Chi Lee; Wayseen Wang
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis.
Taiwanese journal of obstetrics & gynecology 2009;48(4):403-7.
2009: Chih-Ping Chen; Schu-Rern Chern; Pei-Chen Wu; Fuu-Jen Tsai; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis.
Taiwanese journal of obstetrics & gynecology 2009;48(4):389-99.
2008: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Hung-Hung Lin; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
Prenatal diagnosis 2008;28(9):865-7.
2008: Chih-Ping Chen; Shuan-Pei Lin; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay.
European journal of medical genetics 2008;51(4):368-72.
2008: Chih-Ping Chen; Yann-Jang Chen; Schu-Rern Chern; Fuu-Jen Tsai; Tung-Yao Chang; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
Prenatal diagnosis 2008;28(5):450-3.
2007: Chih-Ping Chen; Fuu-Jen Tsai; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p.
Prenatal diagnosis 2007;27(12):1170-3.
2006: Chih-Ping Chen; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Wayseen Wang
Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
Fertility and sterility 2006;86(5):1514.e1-2.
2006: Chih-Ping Chen; Tzu-Hao Wang; Shuan-Pei Lin; Schu-Rern Chern; M-R Chen; Chen-Chi Lee; Yann-Jang Chen; Wayseen Wang
24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism.
European journal of medical genetics 2006;49(6):516-9.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yann-Jang Chen; Schu-Rern Chern; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.
American journal of medical genetics. Part A 2006;140(14):1594-600.
2006: Chih-Ping Chen; Schu-Rern Chern; Chyi-Chyang Lin; Tzu-Hao Wang; Yueh-Chun Li; Lie-Jiau Hsieh; Chen-Chi Lee; Hui-Min Hua; Wayseen Wang
Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Prenatal diagnosis 2006;26(4):313-20.
2006: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Prenatal diagnosis 2006;26(2):138-46.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang
Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
Genetic counseling (Geneva, Switzerland) 2006;17(3):301-6.
2006: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chen-Chi Lee; Jon-Kway Huang; Wayseen Wang
Direct transmission of the 18q- syndrome from mother to daughter.
Genetic counseling (Geneva, Switzerland) 2006;17(2):185-9.
2006: Chih-Ping Chen; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Li-Feng Chen; Meng-Shan Lee; Chen-Wen Pan; Wayseen Wang
Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesis.
Genetic counseling (Geneva, Switzerland) 2006;17(1):91-5.
2006: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Lie-Jiau Hsieh; Jon-Kway Huang; Chen-Chi Lee; Wayseen Wang
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Genetic counseling (Geneva, Switzerland) 2006;17(1):57-63.
2005: Chih-Ping Chen; Schu-Rern Chern; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Tzu-Hao Wang; Chen-Chi Lee; Chen-Wen Pan; Lie-Jiau Hsieh; Wayseen Wang
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.
American journal of medical genetics. Part A 2005;139A(2):146-50.
2005: Chih-Ping Chen; Schu-Rern Chern; Jin-Chern Sheu; Shuan-Pei Lin; Chin-Yuan Hsu; Tung-Yao Chang; Chen-Chi Lee; Wayseen Wang; Hsiao-En Cindy Chen
Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.
Prenatal diagnosis 2005;25(6):502-6.
2005: Chih-Ping Chen; Schu-Rern Chern; Tzu-Hao Wang; Ding-Wei Hsueh; Chen-Chi Lee; Dai-Dyi Town; Wayseen Wang; Tsang-Ming Ko
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Prenatal diagnosis 2005;25(6):492-6.
2005: Chih-Ping Chen; Tung-Yao Chang; Chin-Yuan Tzen; Wayseen Wang; Chen-Chi Lee
Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter).
Prenatal diagnosis 2005;25(3):263-4.
2005: Chih-Ping Chen; Shuan-Pei Lin; Chyi-Chyang Lin; Yueh-Chun Li; Schu-Rern Chern; Wei-Min Chen; Chen-Chi Lee; Lie-Jiau Hsieh; Wayseen Wang
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Prenatal diagnosis 2005;25(2):112-8.
2005: Chih-Ping Chen; Schu-Rern Chern; Chen-Ju Lin; Chen-Chi Lee; Wayseen Wang; Chin-Yuan Tzen
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly.
Genetic counseling (Geneva, Switzerland) 2005;16(1):49-57.
2004: Chih-Ping Chen; Chyi-Chyang Lin; Yueh-Chun Li; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Men-Shan Lee; Wayseen Wang; Chin-Yuan Tzen
Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.
Prenatal diagnosis 2004;24(10):767-73.
2004: Chih-Ping Chen; Schu-Rern Chern; Shojen Cheng; Tung-Yao Chang; Li-Fan Yeh; Chen-Chi Lee; Chen-Wen Pan; Wayseen Wang; Chin-Yuan Tzen
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.
Prenatal diagnosis 2004;24(6):455-62.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of interstitially satellited 6p.
Prenatal diagnosis 2004;24(6):430-3.
2004: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis of the distal 11q deletion and review of the literature.
Prenatal diagnosis 2004;24(2):130-6.
2004: Chih-Ping Chen; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Lee; Wayseen Wang
Discrepancy between the fetus and extra-embryonic tissues in prenatally detected mosaic distal 5p deletion.
Genetic counseling (Geneva, Switzerland) 2004;15(4):473-6.
2004: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Chen-Chi Lee; Jon-Kway Huang; Wayseen Wang; You-Wei Liao
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
Genetic counseling (Geneva, Switzerland) 2004;15(4):437-42.
2004: Chih-Ping Chen; Jin-Chung Shih; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin.
Prenatal diagnosis 2004;24(1):63-6.
2004: Chih-Ping Chen; Chen-Chi Lee; Tung-Yao Chang; Dai-Dyi Town; Wayseen Wang
Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.
Prenatal diagnosis 2004;24(1):50-7.
2004: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Tung-Yao Chang; Wayseen Wang; Chin-Yuan Tzen
Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Prenatal diagnosis 2004;24(1):38-44.
2004: Chih-Ping Chen; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang; Chin-Yuan Tzen
Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
Prenatal diagnosis 2004;24(1):19-25.
2003: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; Daniel T H Chin; Chin-Yuan Tzen; Wayseen Wang
Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Prenatal diagnosis 2003;23(9):758-61.
2003: Chih-Ping Chen; Shuan-Pei Lin; Schu-Rern Chern; Shin-Lin Shih; Chen-Chi Lee; Wayseen Wang; You-Wei Liao
Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Prenatal diagnosis 2003;23(6):504-8.
2003: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chin-Yuan Tzen; Chen-Chi Lee; Wen-Lin Chen; Meng-Shan Lee; Wayseen Wang
Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
Prenatal diagnosis 2003;23(5):375-9.
2003: Chih-Ping Chen; Yuh-Ming Hwu; Li-Fan Yeh; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang
Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion.
Fertility and sterility 2003;79(5):1231-3.
2003: Chih-Ping Chen; Schu-Rern Chern; Tung-Yao Chang; Chen-Chi Lee; Li-Feng Chen; Chin-Yuan Tzen; Wayseen Wang; Chen-Ju Lin; Brian P T Yang; Lawrence S T Yang
Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
Prenatal diagnosis 2003;23(1):40-3.
2002: Chih-Ping Chen; Tung-Yao Chang; Jin-Chung Shih; Shuan-Pei Lin; Chen-Ju Lin; Wayseen Wang; Chen-Chi Lee; Dai-Dyi Town; Chen-Wen Pan; Chin-Yuan Tzen
Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.
Prenatal diagnosis 2002;22(12):1063-6.
2001: Chih-Ping Chen; Schu-Rern Chern; Wayseen Wang; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Tung-Yao Chang; Chin-Yuan Tzen
Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2001;21(5):346-50.
2001: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly.
Prenatal diagnosis 2001;21(2):102-5.
2000: Chih-Ping Chen; Schu-Rern Chern; C L Chang; Chen-Chi Lee; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Prenatal diagnosis 2000;20(9):754-7.
2000: Chih-Ping Chen; koenraad devriendt; Schu-Rern Chern; Chen-Chi Lee; Wayseen Wang; Shuan-Pei Lin
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Prenatal diagnosis 2000;20(5):384-9.
1999: Chih-Ping Chen; koenraad devriendt; Chen-Chi Lee; Wen-Lin Chen; Wayseen Wang; Tao-Yeuan Wang
Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Prenatal diagnosis 1999;19(10):986-9.
1999: Chih-Ping Chen; Jin-Chung Shih; Chen-Chi Lee; Li-Feng Chen; Wayseen Wang; Tao-Yeuan Wang
Prenatal diagnosis of a fetus with distal 10q trisomy.
Prenatal diagnosis 1999;19(9):876-8.
1999: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town; Wen-Lin Chen; Wayseen Wang
Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2).
Prenatal diagnosis 1999;19(8):783-6.
1998: Chih-Ping Chen; Chen-Chi Lee; Chen-Wen Pan; T Y Kir; B F Chen
Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosis.
Prenatal diagnosis 1998;18(12):1289-93.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Wen-Lin Chen; M H Chen; K M Chang
De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.
Journal of medical genetics 1998;35(12):1050-3.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Dai-Dyi Town
Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence.
Prenatal diagnosis 1998;18(10):1068-74.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; CY Chuang
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.
Prenatal diagnosis 1998;18(5):490-5.
1998: Chih-Ping Chen; Schu-Rern Chern; Chen-Chi Lee; Li-Feng Chen; CY Chuang; M H Chen
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus.
Prenatal diagnosis 1998;18(4):393-8.
1997: Chih-Ping Chen; Chen-Chi Lee; Li-Feng Chen; CY Chuang; SW Jan; B F Chen
Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly.
Journal of medical genetics 1997;34(9):777-8.
1997: Chih-Ping Chen; Chyi-Chyang Lin; CY Chuang; Chen-Chi Lee; Wen-Lin Chen; SW Jan; Shuan-Pei Lin
Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21).
Prenatal diagnosis 1997;17(7):675-80.
1997: Chih-Ping Chen; Schu-Rern Chern; FF Liu; SW Jan; Chen-Chi Lee; Y C Chang; C T Yue
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results.
Prenatal diagnosis 1997;17(6):571-6.
1997: Chih-Ping Chen; Chen-Chi Lee; FF Liu; SW Jan; M H Lin; B F Chen
Prenatal diagnosis of cephalothoracopagus janiceps monosymmetros.
Prenatal diagnosis 1997;17(4):384-8.