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Pediatrics-Embryology
Pediatrics-Embryology

... n. Embryos with monosomy (missing one chromosome) usually die XVI. Turner’s Syndrome a. About 1 percent of monosomy X females survive and the incidence of Turner’s syndrome in newborn females is 1/8000 births b. The phenotype of Turner’s is female and secondary sex characteristics in affected female ...
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Heredity – the passing of traits from parents to offspring

... DNA – cellular material with all the information about what traits a living thing may have Chromosome – thread like structures that organize DNA, each chromosome is a long DNA molecule (about 1.5 meters!) Gene – part of the DNA molecule that carries a specific trait (composed of 2 alleles) (ex. flow ...
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... *DOMINANT is represented by a CAPITAL letter; recessive is represented by a lowercase letter *For example – for HEIGHT of a pea plant Tall is dominant and represented with a capital T Short is recessive and represented with a lowercase t ...
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Relative Rates of Nucleotide Substitution in Frogs
Relative Rates of Nucleotide Substitution in Frogs

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DNA - NRF IR Repository
DNA - NRF IR Repository

... DNA stands for DeoxyriboNucleic Acid. It is a molecule that constitutes the genetic material of the cell. It is found in the chromosomes in the nucleus of the cell, as well as in other cellular organelles like the mitochodria in animals and chloroplasts in plants. DNA is the biological code that con ...
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chapter outline - McGraw Hill Higher Education
chapter outline - McGraw Hill Higher Education

... a. Part of the plasmid is transferred first b. Chromosomal genes are transferred next c. The rest of the plasmid is transferred last 4. Complete transfer of the chromosome takes approximately 100 minutes, but the conjugation bridge does not usually last that long; therefore, the entire F factor is n ...
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Mitochondrial DNA



Mitochondrial DNA (mtDNA or mDNA) is the DNA located in mitochondria, cellular organelles within eukaryotic cells that convert chemical energy from food into a form that cells can use, adenosine triphosphate (ATP). Mitochondrial DNA is only a small portion of the DNA in a eukaryotic cell; most of the DNA can be found in the cell nucleus and, in plants, in the chloroplast.In humans, mitochondrial DNA can be assessed as the smallest chromosome coding for 37 genes and containing approximately 16,600 base pairs. Human mitochondrial DNA was the first significant part of the human genome to be sequenced. In most species, including humans, mtDNA is inherited solely from the mother.The DNA sequence of mtDNA has been determined from a large number of organisms and individuals (including some organisms that are extinct), and the comparison of those DNA sequences represents a mainstay of phylogenetics, in that it allows biologists to elucidate the evolutionary relationships among species. It also permits an examination of the relatedness of populations, and so has become important in anthropology and field biology.
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