Search Results - Shun-Ping Chang

Prenatal diagnosis of partial monosomy 21q (21q22.1→qter) associated with intrauterine growth restriction and corpus callosum dysgenesis by Ying-Chung Chen, Wan-Ju Wu, Shun-Ping Chang, Gwo-Chin Ma, Ming Chen

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Phenotype and Genotype of Two Taiwanese Cystic Fibrosis Siblings and a Survey of Delta F508 in East Asians by Chao-Jen Lin, Shun-Ping Chang, Yu-Yuan Ke, Han-Yao Chiu, Lon-Yen Tsao, Ming Chen

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Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients by Ming-Ching Shen, Shun-Ping Chang, Dong-Jay Lee, Wen-Hsiang Lin, Ming Chen, Gwo-Chin Ma

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Prenatal Diagnosis of Autosomal Recessive Renal Tubular Dysgenesis with Anhydramnios Caused by a Mutation in the <i>AGT</i> Gene by Gwo-Chin Ma, Ying-Chung Chen, Wan-Ju Wu, Shun-Ping Chang, Ting-Yu Chang, Wen-Hsiang Lin, Ming Chen

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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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Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome by Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Shun-Ping Chang, Yi-Yung Chen, Pei-Chen Wu, Li-Feng Chen, Wayseen Wang

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Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in <i>PPIB</i> Gene Clustered in Two Taiwanese Families Exhi... by Ting-Yu Chang, I-Fang Chung, Wan-Ju Wu, Shun-Ping Chang, Wen-Hsiang Lin, Norman A. Ginsberg, Gwo-Chin Ma, Ming Chen

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Differential Expression of NUDT9 at Different Phases of The Menstrual Cycle and in Different Components of Normal and Neoplastic Human Endometrium by Ling-Yun Chen, Tze-Ho Chen, Pao-Ying Wen, Chia-Hung Chou, Tsung-Ho Ying, Shun-Ping Chang, Gwo-Chin Ma, Ming Chen

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21 by Chih-Ping Chen, Ming Chen, Schu-Rern Chern, Shun-Ping Chang, Shin-Wen Chen, Shih-Ting Lai, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang

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Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertso... by Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Shun-Ping Chang, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15 by Chih-Ping Chen, Ming Chen, Yi-Ning Su, Schu-Rern Chern, Peih-Shan Wu, Shun-Ping Chang, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang

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Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Mic... by Tien-Yu Yao, Wan-Ju Wu, Kim-Seng Law, Mei-Hui Lee, Shun-Ping Chang, Dong-Jay Lee, Wen-Hsiang Lin, Ming Chen, Gwo-Chin Ma

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Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepa... by Chih-Ping Chen, Ming Chen, Gwo-Chin Ma, Shun-Ping Chang, Fang-Tzu Wu, Yen-Ting Pan, Schu-Rern Chern, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 by Chih-Ping Chen, Ming Chen, Pu-Tsui Wang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Peih-Shan Wu, Shun-Ping Chang, Chen-Wen Pan, Wayseen Wang

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Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9 by Chih-Ping Chen, Ming Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Shun-Ping Chang, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review by Chih-Ping Chen, Ming Chen, Chia-Hsun Wu, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Shun-Ping Chang, Li-Feng Chen, Wayseen Wang

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Preimplantation and prenatal genetic diagnosis of aromatic L-amino acid decarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reac... by Shou-Jen Kuo, Gwo-Chin Ma, Shun-Ping Chang, Hsin-Hung Wu, Chih-Ping Chen, Tung-Ming Chang, Wen-Hsiang Lin, Sheng-Hai Wu, Mei-Hui Lee, Wuh-Liang Hwu, Ming Chen

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Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment by Hsin-Lin Chen, Pei-Hsuan Lin, Yu-Ting Chiang, Wen-Jie Huang, Chi-Fang Lin, Gwo-Chin Ma, Shun-Ping Chang, Jun-Yang Fan, Shin-Yu Lin, Chen-Chi Wu, Ming Chen

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Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay by Chih-Ping Chen, Sheng Chiang, Kung-Liahng Wang, Fu-Nan Cho, Ming Chen, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Shun-Ping Chang, Weu-Lin Chen, Wayseen Wang

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Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements by Chih-Ping Chen, Ming Chen, Yi-Ning Su, Jian-Pei Huang, Gwo-Chin Ma, Shun-Ping Chang, Schu-Rern Chern, Yu-Ting Chen, Jun-Wei Su, Chen-Chi Lee, Dai-Dyi Town, Wayseen Wang

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