Showing 1 - 16 results of 16 for search 'Liang-Liang Fan', query time: 0.14s Refine Results
  1. 1
    Corrigendum: Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A
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  2. 2
    Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13A
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    Article
  3. 3
    Case Report: Exome Sequencing Identified a Novel Frameshift Mutation of α-Actin 1 in a Chinese Family With Macrothrombocytopenia and Mild Bleeding
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  4. 4
    Case Report: A Homozygous Mutation (p.Y62X) of Phospholipase D3 May Lead to a New Leukoencephalopathy Syndrome
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  5. 5
    The formation of droplet encapsulating particles in a Y-typed microchannel
    by Qing Wang, Qi Liu, Liang-Liang Fan, Liang Zhao
    Published 2021-04-01
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  6. 6
    MITF p.Arg217Thr Variant Identified in a Han Chinese Family with Tietz/Waardenburg Syndrome
    by Rong Yu, Lv Liu, Ya-Li Li, Liang-Liang Fan
    Published 2021-01-01
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    Article
  7. 7
    A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient
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  8. 8
    A Novel Nonsense Mutation of ABCA8 in a Han-Chinese Family With ASCVD Leads to the Reduction of HDL-c Levels
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  9. 9
    A Novel Heterozygous Variant in F2 Gene in a Chinese Patient With Coronary Thrombosis and Acute Myocardial Infarction Leads to Antithrombin Resistance
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  10. 10
    Identification of a Novel Variant of ARHGAP29 in a Chinese Family with Nonsyndromic Cleft Lip and Palate
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  11. 11
    Novel Compound Heterozygous DST Variants Causing Hereditary Sensory and Autonomic Neuropathies VI in Twins of a Chinese Family
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  12. 12
    Whole-Exome Sequencing Identified a Novel Homozygous Frameshift Mutation of HPS3 in a Consanguineous Family with Hermansky-Pudlak Syndrome
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  13. 13
    Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome
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  14. 14
    Whole-Exome Sequencing Identifies a Novel TRPM4 Mutation in a Chinese Family with Atrioventricular Block
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  15. 15
    Identification of a novel mutation of NOG in family with proximal symphalangism and early genetic counseling
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  16. 16
    A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel’s deformity
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