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  1. 141
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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

    Published 2010
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  2. 142
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    4q27 deletion and 7q36.1 microduplication in a patient with multiple malformations and hearing loss: a case report by Maolan Wu, Xiangrong Zheng, Xia Wang, Guoyuan Zhang, Jian Kuang

    Published 2020
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  3. 143
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    Antioxidants in Animal Nutrition: UHPLC-ESI-Q<i>q</i>TOF Analysis and Effects on In Vitro Rumen Fermentation of Oak Leaf Extracts by Marialuisa Formato, Alessandro Vastolo, Simona Piccolella, Serena Calabrò, Monica Isabella Cutrignelli, Christian Zidorn, Severina Pacifico

    Published 2022
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  4. 144
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    Prognostic Factors of Pediatric Acute Myeloid Leukemia Patients with t(8;21) (q22;q22): A Single-Center Retrospective Study by Jiapeng Yang, Xiaohua Zhu, Honghong Zhang, Yang Fu, Zifeng Li, Ziping Xing, Yi Yu, Ping Cao, Jun Le, Junye Jiang, Jun Li, Hongsheng Wang, Xiaowen Zhai

    Published 2024
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  5. 145
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    Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis by Chih-Ping Chen, Kuo-Gon Wang, Hsu-Kuang Huang, Cheng-Ran Peng, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang

    Published 2017
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  6. 146
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    COVID-19 and vaccination induced changes in hospital activity in Malta, Q1 2020 to Q1 2021: a population-based study by Sarah Cuschieri, David Borg, Steve Agius, Hagen Scherb, Victor Grech

    Published 2022
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  7. 147
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    A Novel 2.3 Mb Microduplication of 9q34.3 Inserted into 19q13.4 in a Patient with Learning Disabilities by Shalinder Singh, Fern Ashton, Renate Marquis-Nicholson, Jennifer M. Love, Chuan-Ching Lan, Salim Aftimos, Alice M. George, Donald R. Love

    Published 2012
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  8. 148
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    Prenatal diagnosis and molecular cytogenetic characterization of inherited chromosome 2q11.1q11.2 microduplication with fetal intrauterine growth retardation by Yan Ma, E. Lei, Yunfan Xu, Yuexiang Feng

    Published 2022
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  9. 149
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    Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis by Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, Yu-Ling Kuo, Peih-Shan Wu, Meng-Shan Lee, Chien-Wen Yang, Wayseen Wang

    Published 2015
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  10. 150
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    Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma by Chih-Ping Chen, Tsang-Ming Ko, Ming-Chao Huang, Schu-Rern Chern, Tan-Wei Lin, Tung-Yao Chang, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang

    Published 2015
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  11. 151
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    Prader-Willi syndrome patient with atypical phenotypes caused by mosaic deletion in the paternal 15q11-q13 region: a case report by Jinying Wu, Meifang Lei, Xuetao Wang, Nan Liu, Xiaowei Xu, Chunyu Gu, Yuping Yu, Wei Liu

    Published 2022
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  12. 152
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    Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound by Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang

    Published 2018
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  13. 153
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    ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancer by Chun-Lin Lin, Xi Tan, Meizhen Chen, Meena Kusi, Chia-Nung Hung, Chih-Wei Chou, Ya-Ting Hsu, Chiou-Miin Wang, Nameer Kirma, Chun-Liang Chen, Ching-Hung Lin, Kate I. Lathrop, Richard Elledge, Virginia G. Kaklamani, Kohzoh Mitsuya, Tim H.-M. Huang

    Published 2020
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  14. 154
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    An economic evaluation of increased uptake in Q fever vaccination among meat and agricultural industry workers following implementation of the National Q Fever Management Program by Michelle Kermode, Karen Yong, Susan Hurley, Barrie Marmion

    Published 2003
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  15. 155
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    Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene by Chih-Ping Chen, Yi-Ning Su, Yu-Ting Chen, Wen-Lin Chen, Lee James Hsu, Wayseen Wang

    Published 2011
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  16. 156
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    Otitis media: a genome-wide linkage scan with evidence of susceptibility loci within the 17q12 and 10q22.3 regions by Tekely Kathleen, Ferrell Robert E, Jung Jeesun, Mandel Ellen M, Casselbrant Margaretha L, Szatkiewicz Jin P, Ray Amrita, Weeks Daniel E

    Published 2009
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  17. 157
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    A novel locus (<it>CORD12</it>) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1 by Meunier Isabelle, Bocquet Béatrice, Hebrard Maxime, Manes Gaël, Coustes-Chazalette Delphine, Sénéchal Audrey, Bolland-Augé Anne, Zelenika Diana, Hamel Christian P

    Published 2011
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  18. 158
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    Prenatal diagnosis of Jacobsen syndrome associated with a distal 11q deletion and a distal 8q duplication by chromosome microarray analysis in a fetus with a de novo unbalanced translocation of 46,XX,der(11)t(8;11)(q24.13;q23.3) and multiple congenital anomalies on fetal ultrasound by Chih-Ping Chen, Jian-Pei Huang, Fang-Tzu Wu, Peih-Shan Wu, Yen-Ting Pan, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang

    Published 2024
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  19. 159
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    IMPLEMENTASI METODE AMM76;Q21;L QUR'Q21;NQ53; DALAM PEMBELAJARAN PENDIDIKAN AGAMA ISLAM :Studi Deskriptif Implementasi Metode AmM77;Q13;l Qur'Q13;nī Dalam Pembelajaran Pendidikan Agama Islam di kelas VII SMP Negeri 40 Bandung by KHAIRIYAH, Alinda

    Published 2012
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  20. 160
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    Coenzyme Q10 and its effects in the treatment of neurodegenerative diseases by Graciela Cristina dos Santos, Lusânia Maria Greggi Antunes, Antonio Cardozo dos Santos, Maria de Lourdes Pires Bianchi

    Published 2009
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