Functional Genomic Analysis Identified Epidermal Growth Factor Receptor Activation as the Most Common Genetic Event in Oral Squamous Cell Carcinoma
SHEU, Jim Jinn-Chyuan, HUA, Chun-Hung, LIN, Chyi-Chyang, HSIEH, Lie-Jiau, WANG, Tian-Li, SHIH, Ie-Ming, TSAI, Fuu-Jen, LEI WAN, LIN, Ying-Ju, LAI, Ming-Tsung, TSENG, Hsien-Chang, JINAWATH, Natini, TSAI, Ming-Hsui, CHANGE, Nai-Wen, LIN, Chin-Fen
Published in Cancer research (Chicago, Ill.) (15.03.2009)
Published in Cancer research (Chicago, Ill.) (15.03.2009)
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Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats
Li, Yueh-Chun, Chien, Shu-Chin, Setlur, Sunita R., Lin, Wei-De, Tsai, Fuu-Jen, Lin, Chyi-Chyang
Published in Journal of the Formosan Medical Association (01.01.2015)
Published in Journal of the Formosan Medical Association (01.01.2015)
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Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q
Chen, Chih‐Ping, Lin, Shuan‐Pei, Lin, Chyi‐Chyang, Chen, Yann‐Jang, Chern, Schu‐Rern, Li, Yueh‐Chun, Hsieh, Lie‐Jiau, Lee, Chen‐Chi, Pan, Chen‐Wen, Wang, Wayseen
Published in American journal of medical genetics. Part A (15.07.2006)
Published in American journal of medical genetics. Part A (15.07.2006)
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Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract
Chang, Yu-Tzu, Chou, I-Ching, Wang, Chung-Hsing, Chin, Zheng-Nan, Kuo, Huang-Tsung, Lin, Chyi-Chyang, Tsai, Chang-Hai, Tsai, Fuu-Jen
Published in Pediatrics and neonatology (01.04.2013)
Published in Pediatrics and neonatology (01.04.2013)
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Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype
Sung, Pi‐Lin, Chang, Sheng‐Ping, Wen, Kuo‐Chang, Chang, Chia‐Ming, Yang, Ming‐Jie, Chen, Lin‐Chao, Chao, Kuan‐Chong, Huang, Chi‐Ying F., Li, Yueh‐Chun, Lin, Chyi‐Chyang
Published in American journal of medical genetics. Part A (01.12.2009)
Published in American journal of medical genetics. Part A (01.12.2009)
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Journal Article
A new familial insertion, ins(18;9)(q12.2;q33.1q31.1) with a 9q31.1-9q33.1 deletion in a girl with a cleft lip and palate
Chien, Shu-Chin, Li, Yueh-Chun, Li, Ling-Hui, Wu, Jer-Yuarn, Hsu, Pei-Ching, Shi, Sue-Lin, Tsai, Fuu-Jen, Lin, Chyi-Chyang
Published in American journal of medical genetics. Part A (01.07.2010)
Published in American journal of medical genetics. Part A (01.07.2010)
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Genomic Alterations in Human Malignant Glioma Cells Associate with the Cell Resistance to the Combination Treatment with Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand and Chemotherapy
LI, Yueh-Chun, TZENG, Ching-Cherng, SONG, Jin H, TSIA, Fuu-Jen, HSIEH, Lie-Jiau, LIAO, Shu-Ju, TSAI, Chang-Hai, VAN MEIR, Erwin G, CHUNHAI HAO, LIN, Chyi-Chyang
Published in Clinical cancer research (01.05.2006)
Published in Clinical cancer research (01.05.2006)
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Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding
Lee, Ni-Chung, Chang, Shun-Ping, Chang, Cheng-Shyong, Chen, Chia-Hsiang, Lee, Dong-Jay, Lin, Chyi-Chyang, Hwu, Wuh-Liang, Chen, Ming
Published in Prenatal diagnosis (01.11.2009)
Published in Prenatal diagnosis (01.11.2009)
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Rare rearrangements: A “jumping satellite” in one family and autosomal location of the SRY gene in an XX male
Chien, Shu‐Chin, Li, Yueh‐Chun, Ho, Ming, Hsu, Pei‐Ching, Teng, Ru‐Hsiou, Lin, Wei‐De, Tsai, Fuu‐Jen, Lin, Chyi‐Chyang
Published in American journal of medical genetics. Part A (01.12.2009)
Published in American journal of medical genetics. Part A (01.12.2009)
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Sumoylation of p45/NF-E2: Nuclear Positioning and Transcriptional Activation of the Mammalian β-Like Globin Gene Locus
Shyu, Yu-Chiau, Lee, Tung-Liang, Ting, Chun-Yuan, Wen, Shau-Ching, Hsieh, Lie-Jiau, Li, Yueh-Chun, Hwang, Jau-lang, Lin, Chyi-Chyang, Shen, C.-K. James
Published in Molecular and Cellular Biology (01.12.2005)
Published in Molecular and Cellular Biology (01.12.2005)
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Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan
Wang, Yi-Chun, Kung, Chiu-Yun, Su, Mao-Chang, Su, Ching-Chyuan, Hsu, Hsiu-Mei, Tsai, Chin-Chu, Lin, Chyi-Chyang, Li, Shuan-Yow
Published in European journal of human genetics : EJHG (01.08.2002)
Published in European journal of human genetics : EJHG (01.08.2002)
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Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly
Sung, Pi-Lin, Chang, Chia-Ming, Chen, Chih-Yao, Wang, Peng-Hui, Chao, Kuan-Chong, Wen, Kuo-Chang, Cheng, Yung-Yung, Li, Yueh-Chun, Lin, Chyi-Chyang
Published in Taiwanese journal of obstetrics & gynecology (01.06.2012)
Published in Taiwanese journal of obstetrics & gynecology (01.06.2012)
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Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21
Chen, Chih-Ping, Lin, Chyi-Chyang, Ko, Tsang-Ming, Tsai, Fuu-Jen, Chern, Schu-Rern, Lee, Chen-Chi, Chen, Yu-Ting, Wu, Pei-Chen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.09.2010)
Published in Taiwanese journal of obstetrics & gynecology (01.09.2010)
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Journal Article
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion
Chen, Chih‐Ping, Chern, Schu‐Rern, Lin, Shuan‐Pei, Lin, Chyi‐Chyang, Li, Yueh‐Chun, Wang, Tzu‐Hao, Lee, Chen‐Chi, Pan, Chen‐Wen, Hsieh, Lie‐Jiau, Wang, Wayseen
Published in American journal of medical genetics. Part A (01.12.2005)
Published in American journal of medical genetics. Part A (01.12.2005)
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Journal Article
Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 22
Chen, Chih-Ping, Lin, Chyi-Chyang, Su, Yi-Ning, Tsai, Fuu-Jen, Chern, Schu-Rern, Lee, Chen-Chi, Chen, Wen-Ling, Chen, Li-Feng, Wu, Pei-Chen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.09.2010)
Published in Taiwanese journal of obstetrics & gynecology (01.09.2010)
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Journal Article
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
Chen, Chih-Ping, Lin, Chyi-Chyang, Su, Yi-Ning, Tsai, Fuu-Jen, Chen, Ju-Ting, Chern, Schu-Rern, Lee, Chen-Chi, Town, Dai-Dyi, Chen, Li-Feng, Wu, Pei-Chen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.06.2010)
Published in Taiwanese journal of obstetrics & gynecology (01.06.2010)
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Journal Article
Prenatal Diagnosis of mos45,X/46,X,+mar in a Fetus With Normal Male External Genitalia and a Literature Review
Chien, Shu-Chin, Chen, Chih-Ping, Lin, Chyi-Chyang, Huang, Li-Chia, Hsieh, Cheng-Tiao, Tsai, Fuu-Jen
Published in Taiwanese journal of obstetrics & gynecology (01.09.2009)
Published in Taiwanese journal of obstetrics & gynecology (01.09.2009)
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Journal Article
Prenatal Diagnosis of Partial Trisomy 3p (3p21→pter) and Partial Monosomy 11q (11q23→qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System
Chen, Chih-Ping, Wang, Tzu-Hao, Lin, Chyi-Chyang, Tsai, Fuu-Jen, Hsieh, Lie-Jiau, Wang, Wayseen
Published in Journal of the Formosan Medical Association (01.10.2008)
Published in Journal of the Formosan Medical Association (01.10.2008)
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