General Objectives

All learning objectives assume that participants have the background knowledge of medical laboratory technicians or technologists.

Participants will develop the following:

  1. An understanding of the inheritance and expression of human blood groups.

  2. A working understanding of the genetic terminology required to be able to function well in the transfusion laboratory.

  3. An understanding of the clinical relevance of genetic concepts.

  4. Knowledge of Internet genetics resources.

  5. Knowledge of current developments and trends in applying genetics to transfusion medicine.

  6. An historical perspective of how genetics has evolved.

  7. An appreciation of the importance of genetics as a foundation of transfusion science theory and practice.

Specific Objectives

Participants will be able to do the following:

  1. Define the following genetic terms (using human blood group systems as examples if relevant) and explain their clinical relevance, where applicable:
    allelediploid number
    of chromosomes
    locusPunnett square
    amorphdominantmeiosisrecessive
    aneuploidydizygotic twinsmitosisrecombinant
    antitheticalfunctional genesmodifying generegulatory gene
    autosomegenemonozygotic twinssex-linked
    balanced polymorphismgene interactionmutationsomatic chromosomes
    beneficial genegenotypenondisjunctionstructural gene
    chimerahaploid number
    of chromosomes
    operatorsuppressor gene
    chromosomeharmful geneoperonsyntenic
    cis positionhemizygouspedigreeteratogen
    co-dominantheterozygousphenotypetransient polymorphism
    consanguinityhomologous chromosomespolymorphismtrans position
    crossing overhomozygousprobandx-linked
    deletionkaryotypeproposita
    deleted phenotypelinkagepropositus

  2. Describe the inheritance and expression of human blood groups (including ABO, Rh, Kell, Duffy, MNSs, and Xga systems) under the following headings:

    1. dominant, recessive or co-dominant genes
    2. autosomal or sex-linked inheritance
    3. indirect gene products (role of transferases)
    4. effect of deletions, amorphs or suppressor genes

  3. Illustrate inheritance of human blood groups by providing phenotypes and genotypes for family members of pedigrees.

  4. Interpret if blood group inheritance patterns are typical or atypical and, if atypical, provide possible explanations.

  5. Interpret whether or not a pedigree demonstrates independent or dependent inheritance (linkage) of any two blood group systems.

  6. Interpret genetic symbols as they appear in pedigrees and differentiate between symbols used to denote phenotypes and genotypes.

  7. Use established conventions for designating blood group antigens, genes, phenotypes, and genotypes.

  8. Identify examples of the following inheritance patterns and be able to solve genotypes and phenotypes problems based on information provided for some members:

    1. sex-linked recessive
    2. sex-linked dominant
    3. autosomal recessive
    4. autosomal dominant

  9. Access WWW pages on genetics and use the resources to retrieve information and solve problems.

  10. Identify scientists who have made major discoveries about genetics.

  11. Discuss current laboratory techniques used in medical genetics and transfusion medicine.

  12. Discuss the significance of a knowledge of genetics in the routine transfusion lab.

Student Assessment

Assessment for Internet-based modules is based on a Pass/Fail status. To receive credit for a module, you must pass each assignment, demonstrate satisfactory performance for participation in the module, and meet module deadlines.

More specifically, assessment is based on these criteria:


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