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  • 511162: Factor II (Prothrombin), DNA Analysis - Labcorp
    Labcorp test details for Factor II (Prothrombin), DNA Analysis Skip to main content Prothrombin Gene Analysis; Prothrombin Gene Mutation; Share; Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC; 511162: Factor II, DNA Analysis: 24476-4: 511194:
  • Factor II Gene Mutation (Prothrombin G20210A) - Labcorp
    Labcorp test details for Factor II Gene Mutation (Prothrombin G20210A) Skip to main content Close Menu Logins Individuals Patients Find a Lab 500582: Factor II Gene Mutation (Prothrombin G20210A) Specimen; Details; Back to Top; Factor II Gene Mutation (Prothrombin G20210A) TEST: 500582 Test number copied CPT: 81240 Print Share
  • Factor II (Prothrombin) G20210A Mutation Analysis - Labcorp
    Molecular-based testing is highly accurate, but as in any laboratory test, diagnostic errors may occur False positive or false negative results may occur for reasons that include genetic variants, blood transfusions, bone marrow transplantation, somatic or tissue-specific mosaicism, mislabeled samples, or erroneous representation of family
  • 086231: Factor II Activity - Labcorp
    Factor II activity in excess of 115% has been associated with an increased risk of thrombosis 6 The G20210A mutation in the prothrombin gene can be associated with increased plasma prothrombin levels 6,9 This polymorphism can be identified in 1% to 2% of the US population, but is highly race-dependent
  • 500660 ThrombAssure™ | Specialty Testing | Laboratory Corporation of . . .
    View All Labcorp Sites TEST: 500660 Test number copied CPT: 81240; 81241 Print Share Test Includes Factor II Gene Mutation (Prothrombin G20210A) , Factor V Leiden Mutation Special Instructions Informed consent required for NY patients Expected Turnaround Time Informed consent for genetic testing Specimen Requirements Specimen
  • 117702: Thrombotic Risk Profile I - Labcorp
    Labcorp test details for Thrombotic Risk Profile I Skip to main content Logins Result Code Name: Dilute Prothrombin Time(dPT) UofM: sec: Result LOINC: 75508-2: Order Code: 117702: Order Code Name: Factor V Leiden Mutation: Result Code: 512256: Result Name: Reviewed by: UofM: Result LOINC: 72486-4: Reflex Table for PTT-LA; Order Code
  • Genetic Thrombophilia - Labcorp
    Genetic testing is useful for the diagnosis or confirmation of MTHFR, factor V Leiden, and the prothrombin 20210 mutations Regardless of clinical status, genetic testing can be definitive because the patient's DNA remains constant Antigen and activity levels must be measured to diagnose the other congenital thrombotic conditions
  • 452322: Labcorp Pan-Heme NGS
    The sensitivity of this assay is 3% variant allele fraction (VAF) for single nucleotide variants (SNV), 5% for insertions deletions (indels) less than 25 base pairs (bp) and 15% indels greater than or equal to 25 bp CNV sensitivity is greater than or equal to two contiguous exons (subset) to whole gene is copy number less than or equal to 0 85 for deletions and greater than or equal to 1 15
  • Prothrombin (Factor II) 20210G→A Mutation Analysis
    Test Code 17909 CPT Code(s) This germline genetic test requires physician attestation that patient consent has been received if ordering medical facility is located in AK, DE, FL, GA, IA, MA, MN, NV, NJ, NY, OR, SD or VT or test is performed in MA Prothrombin (Factor II) 20210G→A Mutation Analysis - Factor II Mutation (G20210A) is
  • Prothrombin ( F2 ) c. *97G gt;A (G20210A) Pathogenic Variant - ARUP Lab
    Background Information for Prothrombin (F2) c *97G>A (G20210A) Pathogenic Variant:Characteristics: The Factor II, c *97G>A (G20210A) pathogenic variant is a common genetic risk factor for venous thrombosis associated with elevated prothrombin levels leading to increased rates of thrombin generation and excessive growth of fibrin clots The expression of Factor II thrombophilia is impacted by





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