Yining

伊寧}}) (1952) |c2 = 固勒扎 |p2 = Gùlèzhā |w2 = |altname3=Ningyuan |s3=宁远 |t3=寧遠 |p3=Níngyuǎn |mnc = ᡤᡡᠯᠵᠠ |mnc_a = Gvlja |mnc_v = Gūlja |mon = Хулж |mong = ᠬᠤᠯᠵᠠ |rus = Кульджа |rusr = Kuldzha |tib = གུལ་ཅ |wylie = gul ca |thdl = |zwpy = |lhasa = |uig = غۇلجا |uly = Ghulja |uyy = Ƣulja |sgs = Ĝulja |usy = Ғулҗа |lang1 = kk |lang1_content =
Құлжа
|lang2 = xal |lang2_content = |lang3 = chg |lang3_content = غولجا |order = st }} Yining (), also known as Ghulja () or Kulja (Kazakh: ), is a county-level city in northwestern Xinjiang, China. It is the administrative seat and largest city of Ili Kazakh Autonomous Prefecture. Historically, Yining is the successor to the ruined city of Almaliq in neighbouring Huocheng County. Yining is the third largest city in Xinjiang after Ürümqi and Korla. Provided by Wikipedia
Showing 1 - 20 results of 119 for search 'Yi Ning', query time: 0.12s Refine Results
  1. 1
    Current Aspects in the Molecular Genetics and Diagnostics of Spinal Muscular Atrophy

    Current Aspects in the Molecular Genetics and Diagnostics of Spinal Muscular Atrophy by Shu-Chin Chien, Yi-Ning Su

    Published 2005
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  2. 2
    PHOX2B Mutation in a Taiwanese Newborn with Congenital Central Hypoventilation Syndrome

    PHOX2B Mutation in a Taiwanese Newborn with Congenital Central Hypoventilation Syndrome by Tzu-Chiang Wang, Yi-Ning Su, Ming-Chi Lai

    Published 2014
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  3. 3
    Lethal fetal stroke in utero

    Lethal fetal stroke in utero by Tzu-Hung Lin, Chien-Nan Lee, Yi-Ning Su

    Published 2013
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  4. 4
    Pelizaeus-Merzbacher Disease, Easily Misdiagnosed as Cerebral Palsy: A Report of a Three-generation Family

    Pelizaeus-Merzbacher Disease, Easily Misdiagnosed as Cerebral Palsy: A Report of a Three-generation Family by Yen-Chun Chen, Wen-Chen Liang, Yi-Ning Su, Yuh-Jyh Jong

    Published 2014
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  5. 5
    Muscle quality index is associated with trouble sleeping: a cross-sectional population based study

    Muscle quality index is associated with trouble sleeping: a cross-sectional population based study by Yanwei You, Yuquan Chen, Qi Zhang, Ning Yan, Yi Ning, Qiang Cao

    Published 2023
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  6. 6
    Lymphomatoid papulosis with DUSP22-IRF4 rearrangement on 6p25-3: A case report

    Lymphomatoid papulosis with DUSP22-IRF4 rearrangement on 6p25-3: A case report by Yi-Ning Mao, Jie-Yang Jhuang, Bo-Jung Chen, Yu-Hung Wu

    Published 2021
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  7. 7
    Prenatal diagnosis of microvillus inclusion disease

    Prenatal diagnosis of microvillus inclusion disease by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Pei-Chen Wu, Wayseen Wang

    Published 2011
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  8. 8
    Septic Shock after Intracervical Laminaria Insertion

    Septic Shock after Intracervical Laminaria Insertion by Shin-Yu Lin, Wen-Fang Cheng, Yi-Ning Su, Chi-An Chen, Chien-Nan Lee

    Published 2006
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  9. 9
    A large-cohort study of 2971 cases of epulis: focusing on risk factors associated with recurrence

    A large-cohort study of 2971 cases of epulis: focusing on risk factors associated with recurrence by Na Zhao, Yelidana Yesibulati, Pareyida Xiayizhati, Yi-Ning He, Rong-Hui Xia, Xiang-Zhen Yan

    Published 2023
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  10. 10
    Split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization

    Split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization by Chin-Jui Wu, Yi-Ning Su, Tzu-Hung Lin, Li-Hui Tseng, Kuang-Han Chao

    Published 2015
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  11. 11
    Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus associated with split hand-foot malformation. Role of EPS15L1 in pathogenesis

    Array comparative genomic hybridization characterization of multiple interstitial deletions involving 7p22.1, 7q11.23, 7q21.3-q22.1, 19p13.3-p12, and 19q13.11-q13.43 in a fetus ass... by Ya-Lien Hsueh, Yi-Ning Su, Hsin-Yu Lin, Chien-Nan Lee, Jin-Chung Shih

    Published 2015
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  12. 12
    Targeted inhibition of methicillin-resistant Staphylococcus aureus biofilm formation by a graphene oxide-loaded aptamer/berberine bifunctional complex

    Targeted inhibition of methicillin-resistant Staphylococcus aureus biofilm formation by a graphene oxide-loaded aptamer/berberine bifunctional complex by Yi Ning, Xiaoqi Wang, Pingan Chen, Shiwu Liu, Jue Hu, Rong Xiao, Ling Li, Fangguo Lu

    Published 2022
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  13. 13
    Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review

    Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review by Chih-Ping Chen, Yi-Ning Su, Tzu-Hung Lin, Tung-Yao Chang, Jun-Wei Su, Wayseen Wang

    Published 2013
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  14. 14
    Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism

    Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013
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  15. 15
    Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome

    Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome by Chih-Ping Chen, Shuan-Pei Lin, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2013
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  16. 16
    Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II

    Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II by Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2012
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  17. 17
    Prenatal diagnosis of directly transmitted benign 4q12-q13.1 quadruplication associated with tandem segmental amplifications of the LPHN3 gene

    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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  18. 18
    Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II

    Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II by Chih-Ping Chen, Yi-Ning Su, Fang-Yu Hung, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

    Published 2012
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  19. 19
    Prenatal diagnosis of proximal femoral focal deficiency: A case report and literature review

    Prenatal diagnosis of proximal femoral focal deficiency: A case report and literature review by Tzu-Hung Lin, Chi-Hsien Chung, Jin-Chung Shih, Chia-Hui Lin, Chien-Nan Lee, Yi-Ning Su

    Published 2013
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  20. 20
    Intraperitoneal and intracardiac transfusion of recurrent fetal erythroblastosis due to anti-M alloimmunization with unfavorable outcome

    Intraperitoneal and intracardiac transfusion of recurrent fetal erythroblastosis due to anti-M alloimmunization with unfavorable outcome by Tzu-Hung Lin, Jin-Chung Shih, Chia-Hui Lin, Shin-Yu Lin, Yi-Ning Su, Chien-Nan Lee

    Published 2012
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