The Resource Human genetics for M-1 students, Robert Tissot, Elliot Kaufman, (electronic resource)

Human genetics for M-1 students, Robert Tissot, Elliot Kaufman, (electronic resource)

Label
Human genetics for M-1 students
Title
Human genetics for M-1 students
Statement of responsibility
Robert Tissot, Elliot Kaufman
Title variation
  • Genetics for M-1 students
  • Human genetics for 1st year students
Contributor
Subject
Genre
Language
eng
Cataloging source
MMU
Illustrations
illustrations
Index
no index present
Literary form
non fiction
Nature of contents
  • dictionaries
  • bibliography
NLM call number
QZ 50
http://library.link/vocab/relatedWorkOrContributorName
  • Tissot, Robert G
  • Kaufman, Elliot R
  • University of Illinois at Chicago
http://library.link/vocab/subjectName
Genetics, Medical
Label
Human genetics for M-1 students, Robert Tissot, Elliot Kaufman, (electronic resource)
Instantiates
Publication
Note
Title from resource title page (UIC, viewed July 21, 2010)
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
Mendelian inheritance -- General background -- Categories of genetic diseases -- population frequencies -- Modes of inheritance -- Mitosis and meiosis -- Meiosis and gametogenesis -- Pedigree construction -- Modes of inheritance -- Autosomal dominant inheritance -- Heterozygous affected phenotype -- Hallmarks -- Punnett square -- Pedigree -- Variable expressivity -- Late onset -- High recurrent mutation rate -- Incomplete penetrance -- Autosomal recessive inheritance -- Introduction -- Hallmarks -- Carrier probabilities in a pedigree -- Effects of consanguinity -- X-linked dominant inheritance -- Hallmarks -- Punnett square -- Pedigree -- Lethality in males -- X-linked recessive inheritance -- Pedigree -- Punnett square -- Hallmarks -- Bayesian probability -- New mutations in genetic lethals -- Sex limited inheritance -- Mitochondrial inheritance -- Imprinting -- Chromosomal inheritance -- Importance -- Karyotype -- Chromosome replication -- Autosomal chromosomal abnormalities -- Meiotic nondisjunction -- Mitotic nondisjunction -- Robertsonian translocation -- Isochrome formation -- Sex chromosome abnormalities -- Lyon hypothesis -- Barr bodies -- Turner syndrome -- Klinefelter syndrome -- XYY and XXX syndromes -- Non-meiotic chromosome abnormalities -- Inversions -- Ring chromosomes -- Translocations (non-Robertsonian) -- Uniparental disomy -- Multifactorial inheritance -- Importance -- Regression to the mean -- Polygenic inheritance -- The multifactorial model -- Concordance -- Threshold model of disease -- Degree of relationship and genes in common -- Two threshold diseases -- Severity of disease and recurrence risk -- Multiple affected offspring and recurrence risk -- Consanguinity -- Hallmarks of multifactorial inheritance -- Linkage and mapping -- Introduction -- X-linkage -- Autosomal linkage -- Population genetics -- Introduction -- Gene and genotype frequencies -- Codominant alleles -- Hardy-Weinberg equilibrium -- Assumptions -- Calculating frequencies -- Evidence that it applies to humans -- Exceptions to Hardy-Weinberg assumptions -- Effect of recurrent mutation -- Effect of selection against the recessive phenotype -- Balance between selection and recurrent mutation -- Balanced polymorphism -- Non-random mating -- Small populations -- X-linked loci
Control code
649530530
Extent
1 online resource
Form of item
electronic
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other physical details
illustrations (some color)
Specific material designation
remote
System control number
(OCoLC)649530530
Label
Human genetics for M-1 students, Robert Tissot, Elliot Kaufman, (electronic resource)
Publication
Note
Title from resource title page (UIC, viewed July 21, 2010)
Bibliography note
Includes bibliographical references
Carrier category
online resource
Carrier category code
cr
Carrier MARC source
rdacarrier
Content category
text
Content type code
txt
Content type MARC source
rdacontent
Contents
Mendelian inheritance -- General background -- Categories of genetic diseases -- population frequencies -- Modes of inheritance -- Mitosis and meiosis -- Meiosis and gametogenesis -- Pedigree construction -- Modes of inheritance -- Autosomal dominant inheritance -- Heterozygous affected phenotype -- Hallmarks -- Punnett square -- Pedigree -- Variable expressivity -- Late onset -- High recurrent mutation rate -- Incomplete penetrance -- Autosomal recessive inheritance -- Introduction -- Hallmarks -- Carrier probabilities in a pedigree -- Effects of consanguinity -- X-linked dominant inheritance -- Hallmarks -- Punnett square -- Pedigree -- Lethality in males -- X-linked recessive inheritance -- Pedigree -- Punnett square -- Hallmarks -- Bayesian probability -- New mutations in genetic lethals -- Sex limited inheritance -- Mitochondrial inheritance -- Imprinting -- Chromosomal inheritance -- Importance -- Karyotype -- Chromosome replication -- Autosomal chromosomal abnormalities -- Meiotic nondisjunction -- Mitotic nondisjunction -- Robertsonian translocation -- Isochrome formation -- Sex chromosome abnormalities -- Lyon hypothesis -- Barr bodies -- Turner syndrome -- Klinefelter syndrome -- XYY and XXX syndromes -- Non-meiotic chromosome abnormalities -- Inversions -- Ring chromosomes -- Translocations (non-Robertsonian) -- Uniparental disomy -- Multifactorial inheritance -- Importance -- Regression to the mean -- Polygenic inheritance -- The multifactorial model -- Concordance -- Threshold model of disease -- Degree of relationship and genes in common -- Two threshold diseases -- Severity of disease and recurrence risk -- Multiple affected offspring and recurrence risk -- Consanguinity -- Hallmarks of multifactorial inheritance -- Linkage and mapping -- Introduction -- X-linkage -- Autosomal linkage -- Population genetics -- Introduction -- Gene and genotype frequencies -- Codominant alleles -- Hardy-Weinberg equilibrium -- Assumptions -- Calculating frequencies -- Evidence that it applies to humans -- Exceptions to Hardy-Weinberg assumptions -- Effect of recurrent mutation -- Effect of selection against the recessive phenotype -- Balance between selection and recurrent mutation -- Balanced polymorphism -- Non-random mating -- Small populations -- X-linked loci
Control code
649530530
Extent
1 online resource
Form of item
electronic
Media category
computer
Media MARC source
rdamedia
Media type code
c
Other physical details
illustrations (some color)
Specific material designation
remote
System control number
(OCoLC)649530530

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