Hasil Pencarian - Xun-Lun Sheng

  • Menampilkan 1 - 11 hasil dari 11
Perbaiki Hasil
  1. 1
    Analysis of retinal hemodynamics in patients with diabetic retinopathy by color Doppler ultrasonography

    Analysis of retinal hemodynamics in patients with diabetic retinopathy by color Doppler ultrasonography oleh Xu-Hui Wang, Jing Xu, Xun-Lun Sheng

    Diterbitkan 2018-01-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  2. 2
    Clinical analysis of high myopia in 320 cases in Ningxia Hui Autonomous Region

    Clinical analysis of high myopia in 320 cases in Ningxia Hui Autonomous Region oleh Jin-Yan Zhu, Wei-Ning Rong, Ya-Ni Liu, Xun-Lun Sheng

    Diterbitkan 2013-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  3. 3
    Spectrum analysis of gene mutations in retinitis pigmentosa and cone-rod dystrophy

    Spectrum analysis of gene mutations in retinitis pigmentosa and cone-rod dystrophy oleh Ying-Hua Ren, Xun-Lun Sheng, Qin Jia, Wei-Ning Rong, Shuang Zhang

    Diterbitkan 2021-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  4. 4
    Identification of a novel FOXL2 mutation in a fourth-generation Chinese family with blepharophimosis-ptosis-epicanthus inversus syndrome

    Identification of a novel FOXL2 mutation in a fourth-generation Chinese family with blepharophimosis-ptosis-epicanthus inversus syndrome oleh Wei-Ning Rong, Mei-Jiao Ma, Wei Yang, Shi-Qin Yuan, Xun-Lun Sheng

    Diterbitkan 2021-04-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  5. 5
    Myopia with X-linked retinitis pigmentosa results from a novel gross deletion of RPGR gene

    Myopia with X-linked retinitis pigmentosa results from a novel gross deletion of RPGR gene oleh Hui-Ping Li, Shi-Qin Yuan, Xiao-Guang Wang, Xun-Lun Sheng, Xiao-Rong Li

    Diterbitkan 2020-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  6. 6
    De novel heterozygous copy number deletion on 7q31.31-7q31.32 involving TSPAN12 gene with familial exudative vitreoretinopathy in a Chinese family

    De novel heterozygous copy number deletion on 7q31.31-7q31.32 involving TSPAN12 gene with familial exudative vitreoretinopathy in a Chinese family oleh Shuang Zhang, Hai-Ming Yong, Gang Zou, Mei-Jiao Ma, Xue Rui, Shang-Ying Yang, Xun-Lun Sheng

    Diterbitkan 2023-12-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  7. 7
    New pathogenic variants of ALMS1 gene in two Chinese families with Alström Syndrome

    New pathogenic variants of ALMS1 gene in two Chinese families with Alström Syndrome oleh Wan-Yu Cheng, Mei-Jiao Ma, Shi-Qin Yuan, Xiao-long Qi, Wei-Ning Rong, Xun-Lun Sheng

    Diterbitkan 2022-09-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  8. 8
    Identification of genetic variants in five chinese families with keratoconus: Pathogenicity analysis and characteristics of parental corneal topography

    Identification of genetic variants in five chinese families with keratoconus: Pathogenicity analysis and characteristics of parental corneal topography oleh Wan-Yu Cheng, Shang-Ying Yang, Xiao-Yu Huang, Fei-Yin Zi, Hui-Ping Li, Xun-Lun Sheng

    Diterbitkan 2022-10-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  9. 9
    Identification of Four Novel Variants and Determination of Genotype–Phenotype Correlations for ABCA4 Variants Associated With Inherited Retinal Degenerations

    Identification of Four Novel Variants and Determination of Genotype–Phenotype Correlations for ABCA4 Variants Associated With Inherited Retinal Degenerations oleh Qing Zhu, Xue Rui, Ya Li, Ya Li, Ya You, Ya You, Xun-Lun Sheng, Bo Lei, Bo Lei

    Diterbitkan 2021-03-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  10. 10
    Identification of a novel p.R1443W mutation in </b><i><b>RP1</b></i><b> gene associated with retinitis pigmentosa </b><i><b>sine pigmento</b>

    Identification of a novel p.R1443W mutation in </b><i><b>RP1</b></i><b> gene associated with retinitis pigmentosa </b><i><b>sine pigmento</b> oleh Li Ma, Xun-Lun Sheng, Hui-Ping Li, Fang-Xia Zhang, Ya-Ni Liu, Wei-Ning Rong, Jian-Ling Zhang

    Diterbitkan 2013-08-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:
  11. 11
    Prevalence and associated factors of corneal blindness in Ningxia in northwest China

    Prevalence and associated factors of corneal blindness in Ningxia in northwest China oleh Xun-Lun Sheng, Hui-Ping Li, Qing-Xia Liu, Wei-Ning Rong, Wen-Zhang Du, Li Ma, Guang-Hui Yan, Run-Qing Ma, Jian-Ling Zhang, Hui-Fang Xu, Wen-Qing Zou, Xiao-Jun Bi

    Diterbitkan 2014-06-01
    Dapatkan teks lengkap
    Artikel
    Simpan ke Daftar
    Disimpan di:

Alat Pencarian: