Hakutulokset - "Molecular Cytogenetics"

Angelman Syndrome: Molecular Cytogenetic Studies Tekijä J Gordon Millichap

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Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization Tekijä Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li -Feng Chen, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of three chromosomal abnormalities with favorable outcomes Tekijä Qiuqing Chen, Zhen Xu, Guoqiang Chen, Sha Liu, Yanzhi Xia

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Application of Molecular Cytogenetic Technique for Rapid Prenatal Diagnosis of Aneuploidies in Iranian Population Tekijä Habib Nasiri, Jila Dastan, Mohammad Hasan Seifi, Noori Dalooi, Saeed Reza Ghaffari

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Prenatal diagnosis and molecular cytogenetic characterization of two hereditary chromosomal duplications with favorable outcomes Tekijä Y.J. Wu, C.J. Yu, W.H. Tian, Z. Xu

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Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature review Tekijä Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Yu-Ling Kuo, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of hereditary chromosomal deletions and duplications with a favorable outcome Tekijä Guoqiang Sun, Lijuan Han, Shuxin Hu, Xu Liu, Bo Wang

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Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome Tekijä 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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Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 8 Tekijä 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

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis Tekijä 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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Prenatal detection and molecular cytogenetic characterization of Xp deletion and Xq duplication: a case report and literature review Tekijä Qing Lin, Chunya Liang, Bole Du, Lijiao Li, Hong Li, Xiaolan Mai, Sheng Li, Wenyu Xu, Cunzhen Wu, Mi Zeng

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Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings Tekijä 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

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Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21 Tekijä Chih-Ping Chen, Chyi-Chyang Lin, Tsang-Ming Ko, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Pei-Chen Wu, Wayseen Wang

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Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 22 Tekijä Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Wen-Ling Chen, Li-Feng Chen, Pei-Chen Wu, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes Tekijä Chih-Ping Chen, Yeou-Lih Wang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Meng-Shan Lee, Chien-Wen Yang, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication Tekijä Chih-Ping Chen, Jian-Pei Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, 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 16 Tekijä Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang

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Molecular cytogenetic analysis of mosaic 45,X/46,X,r(X) at amniocentesis in a fetus with hydrops fetalis Tekijä Chih-Ping Chen

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21 Tekijä 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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Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis Tekijä Qiao-Fang Hou, Dong Wu, Yan Chu, Shi-Xiu Liao

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