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ARMD-301 搜索结果

  • [ARMD-301]麗花[MIDD-266]作品及种子搜索

    [ARMD-301]麗花[MIDD-266]作品及种子搜索下载
    2021-03-21 15:30:00

    [ARMD-301]发行于2007-03-13时长60分钟出品商是アロマ企画,ARMD-301作品种子搜索下载,麗花[MIDD-266]发行于2007-03-13时长119分钟出品商是ムーディーズ,MIDD-266作品种子搜索下载

  • TCT mapping

    TCT mapping
    2021-07-01 16:00:00

    972 (3CC) CHARACTER 80 TCTARMD(0) - TCT ARM Data 972 (3CC) CHARACTER 16 TCTARNM Element Name 988 (3DC) CHARACTER 8 TCTARTP Element Type 996 (3E4) CHARACTER 16 TCTARRG Restart Group for Element 1012 (3F4) ...

  • Cyber-Physical Systems (CPS) (nsf15541) | NSF –

    Cyber-Physical Systems (CPS) (nsf15541) | NSF –
    2014-12-31 16:00:00

    Yuri Gawdiak, Manager of Strategic Analysis, NASA ARMD, telephone: (202) 358-1853, email: [email protected] Vinay Pai, Program Director, NIH/NIBIB, telephone: (301) 451-4781, email: [email protected] ...

  • ggzyjyzx.tl.gov.cn/tlsggzy/ReadAttachFile.aspx?GongGaoType=...

    ggzyjyzx.tl.gov.cn/tlsggzy/ReadAttachFile.aspx?GongGaoType=...
    2020-05-29 16:00:00

    vdivbKPXxarMdGFdd6Jdh4fRB2YRS0bG6U284PhwX6SVz5NHUjpR9OJho3MprR5IPtovLAO5tdtMbX6cMZM4Tym2P3LhMDyOD3R...PMlK8P6ccQRPbSVRQHp4vCE5HWNfbEjnlfv5PD5x20yebnLdtF301TbVvLdOLgLGo885G57qwusczs3HfVTy+X5N3LFeOGeTuPij...

  • a_第120页_有道词典

    a_第120页_有道词典
    2022-06-09 16:00:00

    第301页 第302页 第303页 第304页 第305页 第306页 第307页 第308页 第309页 第310页 第311页 第312页 ...armaturecircuit armaturedrum armatureendslug armbrust armd armed armdick ue adj armed a armed combat armed forces...

  • EFEMP1 Gene - GeneCards | FBLN3 Protein | FBLN3

    EFEMP1 Gene - GeneCards | FBLN3 Protein | FBLN3
    2021-12-31 16:00:00

    This gene encodes a member of the fibulin family of extracellular matrix glycoproteins. Like all members of this family, the encoded protein contains tandemly repeated epidermal growth factor-like repeats followed by a C-...

  • FBLN5 - Fibulin-5 precursor - Homo sapiens (Human) -

    FBLN5 - Fibulin-5 precursor - Homo sapiens (Human) -
    2021-12-28 16:00:00

    Neuropathy, hereditary, with or without age-related macular degeneration (HNARMD)2 Publications The disease is caused by variants affecting the gene represented in this entry. Disease descriptionAn autosomal dominant neuropathy ...

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