mcgraw hill connect genetics answers

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Learn vocabulary, terms, and more with flashcards, games, and other study tools. the use of DNA manipulation techniques to produce multiply copies of a single gene or segment of DNA, the technique used to fertilize egg cells outside the female's body, a molecule of DNA that includes genetic material from different sources, the process of producing genetically identical organisms, the process of breeding plants and animals for desirable traits, an undifferentiated cell that can develop and become specialized into different cell types of the body, the process of replacing an egg cell's nucleus with the nucleus from a somatic donor cell to produce a cell line of genetically identical cells, The specific fertilization of a male and female gamete of specific genetic origin, A trait that always appears when an individual has an allele for it, The offspring of a cross between the F1 generation, The combination of alleles for any given trait or entire genetic make-up, Traits determined by pairs of allels that segregate during meiosis so that each gamete receives one allele, A cross of tow individuals that differ by one trait, The parent generation the organisms initially crossed, The physical and physiological traits of an organism, A trait that only appears when tow alleles are present for it, A specific characteristics or feature exhibited by an organism, Organisms that exhibit the same traits generation after generation, Traits determined by genes are inherited through the movement of chromosomes during meiosis, A cross of two individuals that differ in two traits due to two different genes, Two alleles for one gene segregate or assort independently of the alleles for other genes during meiosis, A grid used to illustrate all possible genotypes and phenotypes of offspring from genetic crosses, A cross between a parent of an unknown genotype and a homozygous recessive parent, A flow chart that uses symbols to show the inheritance patterns of traits in a family over many generations, The inheritance of traits determined by genes of the autosomal chromosomes 1 to 22 in humans, The inheritance of the dominant phenotype whose genes on the autosomal chromosome, The inheritance of a recessive phenotype is gene is on the autosomal chromosome, A healthcare professional with specialized training in medical genetics and counseling, A technique and treating genetic disorders by introducing the correct form of the defective gene into a parent's genome, A condition in which neither allele for gene completely conceals the presence of the other it results in intermediate expression of a trait, The condition in which both alleles for a trade are you cool expression a heterozygous both alleles are dominant, A survival benefit for individuals who inherit two different alleles for the same trait, A range of variation in one trait resulting from the activity of many genes, A trait that is controlled by more than one gene, Games that are on the same chromosome and that tend to be inherited together, At rate controlled by genes on the X or Y chromosome, A field of study that deals with using computer technology to create and analyze large databases of information, The study of genomes and the complex interactions of genes that result in phenotype, The complete genotype of an individual including various mutations. the process in animals by which an egg that has been fertilized artificially is transferred into a recipient female's uterus. 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Start studying chapter 4-6 unit2 McGraw-Hill biology 11 (genetics). a chromosome that is not involved in determining the sex of an organism, the region where two sister chromatids are held together in a chromosome, a structure that helps to form the spindle fibres, a structure in the nucleus that contains DNA, a part of a chromosome that governs the expression of a trait and is passed on to offspring: it has a specific DNA sequence, the field of biology that involves the study of heredity and variation of living organisms and how genetic information is passed from one generation to the next, a chromosome that contains the same sequence of genes as another chromosome, a photograph of pairs of homologous chromosomes in a cell, an X or Y chromosome, which determines the genetic sex of an organism, one of two chromosomes that are genetically identical and held together at the centromere, a plant or animal cell that forms the body of the organism; excludes reproductive cells, a microtubule structure that facilitates the movement of chromosomes within a cell, reproduction that requires only one parent and produces genetically identical offspring, the exchange of chromosomal segments between a pair of homologous chromosomes, describes a cell that contains pairs of homologous chromosomes, the joining of male and female haploid gametes, a male or female reproductive cell; a haploid sex cell (egg or sperm), describes a cell that contains half the number of chromosomes as the parent cell, the cellular process that produces cells containing half the number of chromosomes as the parent cell; the process of cell division that produces haploid sex cells (egg or sperm), the loss of a chromosome as a result of non-disjunction, the failure of homologous chromosome pairs or sister chromatids to separate during meiosis, oogenesis (OH-oh-gen-uh-sis or OO-oh-gen-uh-sis), the process of producing female gametes (eggs) in mammals, reproduction that requires two parents and produces genetically distinct offspring, the process of producing male gametes (sperm) in mammals, the aligning of homologous chromosomes during prophase I in meiosis I, the gain of an extra chromosome as a result of non-disjunction, a diploid cell formed by the fusion of two gametes, the process by which sperm are collected and concentrated before being introduced into the female's reproductive tract, a process that produces identical copies of genes, cells, or organisms. 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