Collagen, type I, alpha 1

Results: 21



#Item
1SEA350Hu 96 Tests Enzyme-linked Immunosorbent Assay Kit For Collagen Type I Alpha 1 (COL1a1) Organism Species: Homo sapiens (Human) Instruction manual FOR IN VITRO AND RESEARCH USE ONLY

SEA350Hu 96 Tests Enzyme-linked Immunosorbent Assay Kit For Collagen Type I Alpha 1 (COL1a1) Organism Species: Homo sapiens (Human) Instruction manual FOR IN VITRO AND RESEARCH USE ONLY

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Source URL: www.cloud-clone.us

Language: English - Date: 2015-07-14 21:52:24
    2Gene Therapy and Molecular Biology Vol 15, page 112 Gene Ther Mol Biol Vol 15, , 2013 An SP1-binding site polymorphism in the COLIAI gene: may be a strong predictor for low

    Gene Therapy and Molecular Biology Vol 15, page 112 Gene Ther Mol Biol Vol 15, , 2013 An SP1-binding site polymorphism in the COLIAI gene: may be a strong predictor for low

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    Source URL: www.gtmb.org

    Language: English - Date: 2014-01-21 06:01:26
    3Search Tips Block 3 Class of 2017 Please be authenticated through CaseWireless, or have VPN open and connected. From the Cleveland Health Sciences Library home page, please click on PubMed Go to Clinical Queries and typ

    Search Tips Block 3 Class of 2017 Please be authenticated through CaseWireless, or have VPN open and connected. From the Cleveland Health Sciences Library home page, please click on PubMed Go to Clinical Queries and typ

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    Source URL: www.case.edu

    Language: English - Date: 2014-11-11 16:16:11
    4Department of Molecular Genetics Massively Parallel Sequencing for Brittle Bone Disorders and Hereditary Rickets Osteogenesis imperfecta (OI) comprises a group of inherited disorders characterized by bone fragility and

    Department of Molecular Genetics Massively Parallel Sequencing for Brittle Bone Disorders and Hereditary Rickets Osteogenesis imperfecta (OI) comprises a group of inherited disorders characterized by bone fragility and

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    Source URL: www.anzbms.org.au

    Language: English - Date: 2015-04-08 23:11:01
    5Department of Molecular Genetics Brittle Bone Disorders and Hereditary Rickets panel by Massively parallel sequencing (MPS) request form Please read the MPS Brittle Bone Disorders and Hereditary Rickets panel informatio

    Department of Molecular Genetics Brittle Bone Disorders and Hereditary Rickets panel by Massively parallel sequencing (MPS) request form Please read the MPS Brittle Bone Disorders and Hereditary Rickets panel informatio

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    Source URL: www.anzbms.org.au

    Language: English - Date: 2015-04-08 23:10:51
    6Basic research Evaluation and identification of damaged single nucleotide polymorphisms in COL1A1 gene involved in osteoporosis Tariq Ahmad Masoodi, Mohammed A. Alsaif, Sulaiman A. Al Shammari, Adel A. Alhamdan

    Basic research Evaluation and identification of damaged single nucleotide polymorphisms in COL1A1 gene involved in osteoporosis Tariq Ahmad Masoodi, Mohammed A. Alsaif, Sulaiman A. Al Shammari, Adel A. Alhamdan

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    Source URL: www.termedia.pl

    Language: English
    7Tulane University Matrix DNA Diagnostics Lab FORM 1- Instructions for submission of specimen for DNA testing The patient should be fully informed about the test. Nature of the test/Methodology: The test detects mutations

    Tulane University Matrix DNA Diagnostics Lab FORM 1- Instructions for submission of specimen for DNA testing The patient should be fully informed about the test. Nature of the test/Methodology: The test detects mutations

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    Source URL: tulane.edu

    Language: English - Date: 2014-07-25 22:19:17
    8Molecular Genetics Service Profile Osteogenesis Imperfecta (OI) Introduction ◊ ◊

    Molecular Genetics Service Profile Osteogenesis Imperfecta (OI) Introduction ◊ ◊

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    Source URL: www.esdn.org

    Language: English - Date: 2009-03-19 12:03:51
    9Microsoft Word - Dr Harrison.docx

    Microsoft Word - Dr Harrison.docx

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    Source URL: orthodontics.uchc.edu

    Language: English - Date: 2011-11-09 09:15:17
    10About the Types of Ehlers-Danlos The types of Ehlers-Danlos syndrome may appear clear and defined, but symptomatology rarely permits easy classification. Although most of the genes responsible are identified, not all of

    About the Types of Ehlers-Danlos The types of Ehlers-Danlos syndrome may appear clear and defined, but symptomatology rarely permits easy classification. Although most of the genes responsible are identified, not all of

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    Source URL: ednf.org

    Language: English - Date: 2013-11-26 10:22:03