يعرض 1 - 20 نتائج من 170 نتيجة بحث عن '"Chien-Wen Yang"', وقت الاستعلام: 0.64s تنقيح النتائج
  1. 1
    Academic Journal
    OrchidBase 6.0: increasing the number of Cymbidium (Orchidaceae) genomes and new bioinformatic tools for orchid genome analysis

    المؤلفون: You-Yi Chen, Ye Sun, Chung-I Li, Shao-Ting Lin, Hao-Chen Zheng, Zhe-Bin Zhang, Bing-Ru Lee, Chun-Lin Hsieh, Yu-Yun Hsiao, Chi-Nga Chow, Chien-Wen Yang, Wen-Chi Chang, Heming Chen, Feng-Xi Yang, Gen-Fa Zhu, Qinyao Zheng, Cheng-Yuan Zhou, Zhuang Zhao, Ye Ai, Lin-Ying Wang, Deqiang Chen, Xin He, Ming-Zhong Huang, Dong-Hui Peng, Hao Yu, Siren Lan, Zhong-Jian Liu, Wei-Sheng Wu, Wen-Chieh Tsai

    المصدر: BMC Plant Biology, Vol 25, Iss 1, Pp 1-13 (2025)

    مصطلحات موضوعية: Orchid, OrchidBase, Cymbidium, Whole-genome sequencing, Genome, Transcriptome, Botany, QK1-989

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/1471-2229

    URL الوصول: https://doaj.org/article/32f524ff812642a4be207b17da16a693

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  2. 2
    Academic Journal
    First-trimester application of expanded non-invasive prenatal testing in the genetic investigation of fetal 1p36 deletion syndrome associated with a familial unbalanced reciprocal translocation of 46,XX,der(1)t(1;2) (p36.2;q37.3)dmat

    المؤلفون: Chih-Ping Chen, Shun-Long Weng, Fang-Tzu Wu, Peih-Shan Wu, Yen-Ting Pan, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 6, Pp 909-912 (2024)

    مصطلحات موضوعية: 1p36 deletion, Expanded NIPT, Partial monosomy 1p (1p36.2→pter), Partial trisomy 2q (2q37.3→qter), Translocation, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455924002420; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/08715fcd276149e3925dea0af7175041

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  3. 3
    Academic Journal
    Low-level mosaic trisomy 7 at amniocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the trisomy 7 cell line and a favorable fetal outcome

    المؤلفون: Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Peih-Shan Wu, Chien-Wen Yang, Chien-Ling Chiu, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 4, Pp 549-551 (2024)

    مصطلحات موضوعية: Amniocentesis, Mosaic trisomy 7, Prenatal diagnosis, UPD 7, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455924001347; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/91a9dae58f294e279c85519676d2a385

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  4. 4
    Academic Journal
    Databases and prospects of dynamic gene regulation in eukaryotes: A mini review

    المؤلفون: Chi-Nga Chow, Chien-Wen Yang, Wen-Chi Chang

    المصدر: Computational and Structural Biotechnology Journal, Vol 21, Iss , Pp 2147-2159 (2023)

    مصطلحات موضوعية: Transcription factor, Histone modification, DNA methylation, Database, Dynamic regulation, Non-coding RNA, Biotechnology, TP248.13-248.65

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S2001037023001319; https://doaj.org/toc/2001-0370

    URL الوصول: https://doaj.org/article/bc9e061283864171a6ecd1c72d8e043e

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  5. 5
    Academic Journal
    The Prevalence and Risk Factors of Hypokalemia in Pregnancy-Related Hospitalizations: A Nationwide Population Study

    المؤلفون: Chien-Wen Yang, Si Li, Yishan Dong

    المصدر: International Journal of Nephrology, Vol 2021 (2021)

    مصطلحات موضوعية: Diseases of the genitourinary system. Urology, RC870-923

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/2090-214X; https://doaj.org/toc/2090-2158

    URL الوصول: https://doaj.org/article/e9595887d592465192489b4e1d2c09f9

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  6. 6
    Academic Journal
    Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound

    المؤلفون: Chih-Ping Chen, Shu-Yuan Chang, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 5, Pp 734-738 (2018)

    مصطلحات موضوعية: Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455918301906; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/39945999891b4e92a281892681836a94

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  7. 7
    Academic Journal
    Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound

    المؤلفون: 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

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 5, Pp 739-744 (2018)

    مصطلحات موضوعية: Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455918301918; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/8ae57f30b6b749df9b942fb1f97d1c03

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  8. 8
    Academic Journal
    Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound

    المؤلفون: Chih-Ping Chen, Shu-Yuan Chang, Liang-Kai Wang, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Dai-Dyi Town, Li-Feng Chen, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 5, Pp 730-733 (2018)

    مصطلحات موضوعية: Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S102845591830189X; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/189856d765324de5b27404e490a842fc

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  9. 9
    Academic Journal
    Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability

    المؤلفون: Chih-Ping Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Chien-Wen Yang, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 4, Pp 578-582 (2018)

    مصطلحات موضوعية: Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455918301360; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/60ee999409744c8492fa68b89de51aa0

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  10. 10
    Academic Journal
    Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities

    المؤلفون: Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 57, Iss 1, Pp 128-132 (2018)

    مصطلحات موضوعية: 17p13.3 microdeletion, CRK, PAFAH1B1, Prenatal diagnosis, YWHAE, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917303169; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/4a54141bf59640fa82c477024449811b

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  11. 11
    Academic Journal
    Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1

    المؤلفون: Chih-Ping Chen, Chih-Heng Hsieh, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 6, Pp 847-851 (2017)

    مصطلحات موضوعية: 18q12.1-q12.3 deletion, CELF4, DTNA, Prenatal diagnosis, SETBP1, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917302668; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/66981e6c033447a1b5d11aeb55600ba1

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  12. 12
    Academic Journal
    Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome

    المؤلفون: Chih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 6, Pp 836-839 (2017)

    مصطلحات موضوعية: Amniocentesis, Mosaic tetrasomy 18p, Prenatal diagnosis, Supernumerary isochromosome 18p, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917302632; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/3c90904020b34f01906290e9f14c3c34

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  13. 13
    Academic Journal
    Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones

    المؤلفون: Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 6, Pp 821-826 (2017)

    مصطلحات موضوعية: 4p16.3 microdeletion, Cleft lip and palate, FGFRL1, TACC3, Wolf-hirschhorn syndrome, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917302607; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/b0eb967f0786448b924b4b6bf5831dcf

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  14. 14
    Academic Journal
    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

    المؤلفون: 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

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 4, Pp 527-533 (2017)

    مصطلحات موضوعية: 9p duplication syndrome, Paternal uniparental disomy 9, Small supernumerary marker chromosome 9, Supernumerary ring chromosome 9, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917301511; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/1f108fbbdd934b0ebff98a154c07377f

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  15. 15
    Academic Journal
    Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect

    المؤلفون: Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 4, Pp 550-553 (2017)

    مصطلحات موضوعية: 15q24.2-q26.2 duplication, Anencephaly, Neural tube defect, Partial trisomy 15q, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917301560; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/cdb7038a1e434ce8943d7195b24609c3

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  16. 16
    Academic Journal
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16

    المؤلفون: 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

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 4, Pp 545-549 (2017)

    مصطلحات موضوعية: 16q11.2-q22.1 duplication, Chromosome 16, Prenatal diagnosis, Small supernumerary marker chromosome, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917301559; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/02c712a0d5e94645a0ea20a6258707e7

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  17. 17
    Academic Journal
    Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome

    المؤلفون: Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 2, Pp 264-267 (2017)

    مصطلحات موضوعية: Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917300268; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/8a4fa858a4934e0db444f5ab7c882d8a

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  18. 18
    Academic Journal
    Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality

    المؤلفون: Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Shin-Wen Chen, Peih-Shan Wu, Chien-Wen Yang, Chen-Chi Lee, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 2, Pp 217-223 (2017)

    مصطلحات موضوعية: 5q13.2 microdeletion, chromosome 4, mosaicism, prenatal diagnosis, small supernumerary marker chromosome, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917300189; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/6b48b17a80e94ecfb49813baed60ab3f

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  19. 19
    Academic Journal
    Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome

    المؤلفون: Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 2, Pp 238-242 (2017)

    مصطلحات موضوعية: amniocentesis, mosaic trisomy 12, prenatal diagnosis, trisomy 12 mosaicism, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455917300220; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/35fa87deb7584d14b30be685084b3280

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  20. 20
    Academic Journal
    Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound

    المؤلفون: Chih-Ping Chen, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chien-Wen Yang, Wayseen Wang

    المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 56, Iss 1, Pp 102-105 (2017)

    مصطلحات موضوعية: chromosome 11q deletion, congenital heart defect, Jacobsen syndrome, Gynecology and obstetrics, RG1-991

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1028455916302431; https://doaj.org/toc/1028-4559

    URL الوصول: https://doaj.org/article/291a17a5ef6540e7a58513bb248bcf5d

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