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  • Chromosome Analysis (Karyotyping) - Testing. com
    Chromosome analysis or karyotyping is a test that evaluates the number and structure of a person's chromosomes in order to detect abnormalities T J (© 2011) Mosby’s Diagnostic and Laboratory Test Reference 10th Edition: Mosby, Inc , Saint Louis, MO Pp 268-269 Since the sex chromosomes (XX or XY) are identified during the
  • Chromosome Analysis, Blood | Test Detail | Quest Diagnostics
    Please provide SERVICE AREA INFORMATION to find available tests you can order In-home collection is not available in your area through Quest Mobile Clinical Significance Chromosome Analysis, Blood - This test may assist with the detection of common chromosome abnormalities Send specimen to testing lab for viability determination Do not
  • Chromosome Analysis - University Hospitals
    If you are male, you have an XY pair If you are female, you have an XX pair The other 22 pairs are called autosomes, and they are the same in males and females you may have a test called fluorescence in situ hybridization (FISH) analysis, which looks at specific parts of your chromosomes 44 autosomes plus 2 X chromosomes for females
  • What to Expect From a Chromosome Analysis Blood Test - Genetics
    A chromosome analysis blood test is usually conducted by drawing a blood sample from the patient The sample is then sent to a laboratory, where the chromosomes are analyzed under a microscope The laboratory technicians will examine the chromosomes for any abnormalities and provide a detailed report of the findings
  • Chromosome Analysis: Purpose, Test Process, and Results - KnowYourDNA
    Some blood cancers, like chronic myeloid leukemia, carry a specific swap between chromosomes 9 and 22 (the “Philadelphia chromosome”) Spotting that change helps doctors confirm the diagnosis and tailor treatment How the Test Works The lab must first grow your cells, then “freeze” them mid-division when chromosomes are easiest to see
  • Fish Analysis, X and Y Chromosomes - Saint Francis Health System
    FISH ANALYSIS, X AND Y CHROMOSOMES Male infertility, Y chromosome translocation, XX Male, Turner syndrome, Opposite-sex bone marrow transplantation TURNAROUND TIME: 7 to 10 days TESTING METHODOLOGY: Fluorescence in situ hybridization A Cytogenetics Laboratory Test Requisition must accompany the specimen Contact the Cytogenetics
  • Epic Code LAB2111439 XX and XY (includes SRY) by FISH - Test Catalog
    Ordering Instructions XX and XY (includes SRY) by FISH is a predictive and presymptomatic genetic test Submission of an order for any predictive genetic tests and presymptomatic genetic tests, as defined by MCL 333 17020, contained in this catalog constitutes certification to Corewell Health laboratories that the ordering physician understands that written, informed consent is required for
  • Karyotype Genetic Test - MedlinePlus
    A karyotype test checks the chromosomes in your cells to: See whether you have a full set of 46 chromosomes Having too many or too few chromosomes can cause serious problems with health, growth, and normal development, such as Down syndrome (extra chromosome 21) and Turner syndrome (missing X chromosome)
  • Karyotype Test: Test What Is It - Cleveland Clinic
    The process to get blood for a standard karyotype test only takes a few minutes You may get the test at your healthcare provider’s office, a hospital or a lab A healthcare provider called a lab technician usually takes blood samples Here’s what you can expect: The lab technician takes blood from a vein in your arm using a thin needle
  • Karyotype Test - Purpose, Results, Normal Range, and more
    A normal karyotype consists of 46 chromosomes, arranged in 23 pairs (22 pairs of autosomes and one pair of sex chromosomes) For females, the sex chromosomes are XX, while for males, they are XY No abnormalities are detected in the number or structure of the chromosomes Abnormal Karyotype An abnormal karyotype may indicate chromosomal disorders





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