Functional Genomic Analysis Identified Epidermal Growth Factor Receptor Activation as the Most Common Genetic Event in Oral Squamous Cell Carcinoma von 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

Volltext

Prenatal detection and characterization of a psu idic(8)(p23.3) which likely derived from nonallelic homologous recombination between two MYOM2-repeats von Li, Yueh-Chun, Chien, Shu-Chin, Setlur, Sunita R., Lin, Wei-De, Tsai, Fuu-Jen, Lin, Chyi-Chyang

Volltext

Prenatal molecular cytogenetic analysis of a mild dysmorphic fetus with a huge unbalance karyotype involving partial 9p deletion and partial 18q duplication von Li, Yueh-Chun, Pan, Yi-Ju, Tsai, Fuu-Jen, Lin, Chyi-Chyang

Volltext

Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q von 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

Volltext

Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract von Chang, Yu-Tzu, Chou, I-Ching, Wang, Chung-Hsing, Chin, Zheng-Nan, Kuo, Huang-Tsung, Lin, Chyi-Chyang, Tsai, Chang-Hai, Tsai, Fuu-Jen

Volltext

Cervid satellite DNA and karyotypic evolution of Indian muntjac von Li, Yueh-Chun, Chung Shan Medical University Hospital, Taichung, Taiwan, Lin, Chyi-Chyang, China Medical University, Taichung, Taiwan

Volltext

Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype von 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

Volltext

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 von Chien, Shu-Chin, Li, Yueh-Chun, Li, Ling-Hui, Wu, Jer-Yuarn, Hsu, Pei-Ching, Shi, Sue-Lin, Tsai, Fuu-Jen, Lin, Chyi-Chyang

Volltext

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... von 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

Volltext

Rare rearrangements: A “jumping satellite” in one family and autosomal location of the SRY gene in an XX male von Chien, Shu‐Chin, Li, Yueh‐Chun, Ho, Ming, Hsu, Pei‐Ching, Teng, Ru‐Hsiou, Lin, Wei‐De, Tsai, Fuu‐Jen, Lin, Chyi‐Chyang

Volltext

Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding von Lee, Ni-Chung, Chang, Shun-Ping, Chang, Cheng-Shyong, Chen, Chia-Hsiang, Lee, Dong-Jay, Lin, Chyi-Chyang, Hwu, Wuh-Liang, Chen, Ming

Volltext

Sumoylation of p45/NF-E2: Nuclear Positioning and Transcriptional Activation of the Mammalian β-Like Globin Gene Locus von 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

Volltext

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, agenesi... von 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

Volltext

Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan von Wang, Yi-Chun, Kung, Chiu-Yun, Su, Mao-Chang, Su, Ching-Chyuan, Hsu, Hsiu-Mei, Tsai, Chin-Chu, Lin, Chyi-Chyang, Li, Shuan-Yow

Volltext

A paternally derived inverted duplication of distal 14q with a terminal 14q deletion von 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

Volltext

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21 von 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

Volltext

Hematopoietically expressed homeobox gene is associated with type 2 diabetes in KK Cg‑Ay/J mice and a Taiwanese Han Chinese population von Lu, Chi-Cheng, Chen, Yng-Tay, Chen, Shih-Yin, Hsu, Yuan-Man, Lin, Chyi-Chyang, Tsao, Je-Wei, Juan, Yu-Ning, Yang, Jai-Sing, Tsai, Fuu-Jen

Volltext

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 22 von 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

Volltext

Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 18 and Associated With a Reciprocal Translocation I... von 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

Volltext

Prenatal Diagnosis of Partial Trisomy 3p (3p21→pter) and Partial Monosomy 11q (11q23→qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pye... von Chen, Chih-Ping, Wang, Tzu-Hao, Lin, Chyi-Chyang, Tsai, Fuu-Jen, Hsieh, Lie-Jiau, Wang, Wayseen

Volltext