Showing 1 - 4 results of 4 for search 'Tengyan Li', query time: 0.02s Refine Results
  1. 1
    A novel missense variant in LAMC1 identified in a POI family by whole exome sequencing

    A novel missense variant in LAMC1 identified in a POI family by whole exome sequencing by Huanfang Xu, Chunyan Wang, Han Wei, Tengyan Li, Yigong Fang, Binbin Wang

    Published 2023
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  2. 2
    NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree

    NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree by Lin Li, Fan Feng, Minying Zhao, Tengyan Li, Wentao Yue, Xu Ma, Binbin Wang, Chenghong Yin

    Published 2020
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  3. 3
    Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency

    Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency by Beili Chen, Lin Li, Jing Wang, Tengyan Li, Hong Pan, Beihong Liu, Yiran Zhou, Yunxia Cao, Binbin Wang

    Published 2018
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  4. 4
    Rare homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous mating family

    Rare homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous mating family by Qiong Xing, Ruyi Wang, Beili Chen, Lin Li, Hong Pan, Tengyan Li, Xu Ma, Yunxia Cao, Binbin Wang

    Published 2020
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