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the study of the mechanism of heredity is called? |
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diploid number of chromosomes is in all cells except what? |
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diploid number = __ (23 pairs of homologous chromosomes) |
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__ pair of sex chromosomes determines the genetic sex (XX = female, XY = male) |
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_____ pairs of autosomes guide expression of most other traits |
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diploid chromosomal complement displayed in homologous pairs is called? |
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genetic (DNA) makeup; two sets of genetic instructions (maternal and paternal) |
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matched genes at the same locus on homologous chromosomes is called? |
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alleles controlling a single trait are the same is called? |
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alleles for a trait are different is called? |
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an allele that masks or suppresses its (recessive) partner is called? |
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the genetic makeup is called? |
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the way the genotype is expressed is called? |
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what are the 3 sexual sources of genetic variation? |
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1)segregation and independent assortment of chromosomes 2)crossover of homologues 3)random fertilization of eggs by sperm |
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during _____________, maternal and paternal chromosomes are randomly distributed to daughter cells |
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gametogenesis occurs during what sexual sources of genetic variation? |
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segregation and independent assortment of chromosomes |
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in segregation and independent assortment, the two alleles of each pair are segregated during what? |
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the number of gamete type = _____, where n is the number of homologous pairs in segregation and independent assortment |
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in a man's testes, 2n = 2 to the 23 power which equals what? |
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what sexual sources of genetic variation where? -genes on the same chromosome are linked -chromosomes can cross over, forming a chiasma, and exchange segments -recombinant chromosomes have mixed contribution from each parent |
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crossover and genetic recombination |
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when a single egg is fertilized by a single sperm in a random manner is know as? |
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because of independent assortment and random fertilization, an offspring represents one out of what zygote possibilities?________________________ |
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72 trillion (8.5 milliion x 8.5 million) |
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most traits are determined by _____________ or by the interaction of several gene pairs |
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what are the 5 types of inheritance? |
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1)dominant-recessive inheritance 2)incomplete dominance 3)multiple-allele inheritance 4)sex-linked inheritance 5)polygene inheritance |
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what reflects the interaction of dominant and recessive alleles and a punnett square is used? |
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dominant-recessive inheritance |
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what predicts the possible gene combinations resulting from the mating of parents of known genotype? |
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widow's peaks, freckles, and dimples are examples of what? |
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dominant disorders are uncommon because? |
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many are lethal and result in death before the reproductive age |
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____________ is caused by delayed-action gene |
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most genetic disorders are inherited as simple recessive traits such as? |
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albinism, cystic fibrous, and tay-sachs disease |
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carries who do not express the trait but can pass it on to their offspring are called? |
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in incomplete dominance, heterozygous individuals have and intermediate phenotype like? |
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sickle-cell trait (both aberrant and normal Hb are made); can suffer a sickle-cell crisis under prolonged reduction of blood O2 |
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sickle-cell anemia (only aberrant Hb is made; more susceptible to sickle-cell crisis) |
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genes that exhibit more than two allele forms with ABO blood grouping as an example is know as what type of inheritance? |
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multiple-allele inheritance |
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three allelea (IA, IB, i) determine the ABO blood type in humans IA and IB are ___________(both are expressed if present), and i is recessive |
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inherited traits determined by genes on the sex chromosomes are know as what type of inheritance? |
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x chromosomes bear over over__________ genes which many are used for brain function |
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Y chromosomes carry about _________ genes |
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what are found only on the X chromosome, typically passed from mothers to sons (e.g., hemophilia or red-green color blindness), and are never masked or damped in males (no Y counterpart)? |
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what type of inheritance depends on several different gene pairs at different locations acting on tandem? |
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what type of inheritance gene results in continuous phenotypic variation between extremes like skin color, eye color, and height? |
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what is used when there is a know risk of a genetic disorder? |
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amniotic fluid is withdrawn after the 14th week and fluid and cells are examined for genetic abnormalities is what fetal testing? |
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chorionic villi are sampled and karyotyped for genetic abnormalities in what fetal testing? |
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chorionic villus sampling (CVS) |
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what are example of two fetal testing? |
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amniocentesis and chorionic villus sampling (CVS) |
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