Search Results - Chen Chi Lee

Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother by Chih-Ping Chen, Tsung-Hsien Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang

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High-level mosaicism for 45,X in 45,X/46,X,+mar at amniocentesis in a pregnancy associated with positive non-invasive prenatal testing for Turner syndrome, normal male external gen... by Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang

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Low-level mosaic trisomy 21 due to mosaic unbalanced Robertsonian translocation of 46,XX,+21,der(21;21) (q10;q10)/46,XX at amniocentesis in a pregnancy associated with a favorable... by Chih-Ping Chen, Yi-Yung Chen, Fang-Tzu Wu, Yen-Ting Pan, Chen-Chi Lee, Wayseen Wang

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First-trimester sonographic demonstration of digynic triploidy by Chih-Ping Chen, Yi-Yung Chen, Schu-Rern Chern, Yu-Ling Kuo, Chen-Chi Lee, Wayseen Wang

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Trisomy 13 Mosaicism Associated With Cyclopia and Cystic Hygroma by Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang

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Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang

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Low-level mosaic trisomy 20 without uniparental disomy 20 at amniocentesis in a pregnancy associated with a favorable outcome, cytogenetic discrepancy between uncultured amniocytes... by Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Schu-Rern Chern, Peih-Shan Wu, Chen-Chi Lee, Wayseen Wang

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A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty... by Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Chen-Chi Lee, Wayseen Wang

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Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive dec... by Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Chen-Chi Lee, Chien-Ling Chiu, Wayseen Wang

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Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 → q11.23 by Array Comparative Genomic Hybridization by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Chin-Yuan Hsu, Chen-Chi Lee, Wayseen Wang

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Down Syndrome Due to Unbalanced Homologous Acrocentric Rearrangements and its Recurrence in Subsequent Pregnancies: Prenatal Diagnosis by Amniocentesis by Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Shu-Shien Chiang, Chen-Chi Lee, Wayseen Wang

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Low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues, perinatal progressive decrease of the trisomy 21 cell line a... by Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Wen-Lin Chen, Chen-Chi Lee, Wayseen Wang

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High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line by Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Yun-Yi Chen, Wayseen Wang

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Incidental detection of familial 8p23.2 microduplication encompassing CSMD1 associated with mosaic 46,XY,t(7;8)(q31.2;p23.1)/46,XY at amniocentesis in a pregnancy with no apparent... by Chih-Ping Chen, Yeou-Lih Wang, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Chen-Chi Lee, Wayseen Wang

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Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Wayseen Wang

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Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with... by Chih-Ping Chen, Ming Chen, Yuh-Ming Hwu, Shun-Ping Chang, Shin-Wen Chen, Shih-Ting Lai, Chen-Chi Lee, Wayseen Wang

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Mosaic distal 9p deletion or 46,XY,del(9)(p23)/46,XY at amniocentesis in a pregnancy associated with perinatal progressive decrease of the aneuploid cell line and a favorable fetal... by Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Chen-Chi Lee, Wen-Lin Chen, Chien-Ling Chiu, Wayseen Wang

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Prenatal diagnosis of a 14-Mb 11p11.2-p13 deletion by chromosome microarray analysis in a pregnancy with fetal recombinant chromosome 11 syndrome of rec(11)del(11)(p11.2p13)ins(11)... by Chih-Ping Chen, Chen-Yu Chen, Fang-Tzu Wu, Peih-Shan Wu, Yen-Ting Pan, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang

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Late-onset fetal bilateral pleural effusions associated with Down syndrome by Shih-Ting Lai, Chih-Ping Chen, Chen-Ju Lin, Chin Yuan Hsu, Peih-Shan Wu, Chen Chi Lee, Chen Wen Pan, Wayseen Wang

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