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Down syndrome is caused by trisomy 21
Down syndrome is caused by trisomy 21

... Down Syndrome and Translocation Heterozygote • Down syndrome is caused by trisomy 21 (3 copies of chromosome 21). • 95% of Down syndrome cases are associated with nondisjunction and shows no familial recurrence. ...
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... Mutations in reproductive cells: ...
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... dominant allele and one recessive, disorder-causing allele, do not have the disorder, but can pass it on because they are carriers of the disorder. • Sex-linked genes: Genes on the sex-chromosomes (the X and Y chromosomes in many species) are sex-linked genes. In mammals, including humans, and some ...
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7.1 Chromosomes and Phenotype KEY CONCEPT affect the expression of traits.

... The chromosomes on which genes are located can affect the expression of traits. ...
Genetics - TeacherWeb
Genetics - TeacherWeb

... body hair, hairy ear rims, SRY gene); only effect men Barr Bodies -In body cells of females one X chromosome at random is turned off early in development; inactivated X is called a Barr body -All the cells descended from that cell have the same X turned off -If female is heterozygous she becomes a m ...
Genes
Genes

... Tay-Sachs Disease: Causes destruction of nervous system, blindness, and death during early childhood. Cystic Fibrosis: Makes breathing and digestion difficult, its caused by abnormal genes, one from each parent. Down Syndrome: Caused by a chromosomal abnormality known as Trisony-21,( the presence of ...
7.1 Chromosomes and Phenotype
7.1 Chromosomes and Phenotype

... • Dominant disorders are less common – Huntingtons disease affects the nervous system, specifically causing brain cells to break down. It occurs in adulthood, and is fatal. • Since it occurs in adulthood someone can pass it on to there children, even before they show symptoms. ...
DeKalb County - Purdue University
DeKalb County - Purdue University

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Chapter 12 DNA and RNA - Northwestern High School

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Chromosomes Eukaryote

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6.5 , 7.1

... People who have one dominant allele and one recessive, disorder-causing allele, do not have the disorder, but can pass it on because they are carriers of the disorder. • Sex-linked genes: Genes on the sex-chromosomes (the X and Y chromosomes in many species) are sex-linked genes. In mammals, includi ...
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R 7.1

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Greatest Discoveries with Bill Nye: Genetics

... 24. In 1997, Fire and Mellow were injecting RNA into the cells of a _______________. ...
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Primary School Presentation - Unique The Rare Chromosome

... Take a minute to think about some of the little differences that make you unique. ...
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Ch. 12.1: DNA stores Information

... Non-disjunction Homologous chromosomes or sister chromatids fail to separate during meiosis. Result: Gametes with abnormal # of chromosomes… Offspring with abnormal # of offspring ...
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Reproduction and Development

... • Mating of two individuals with contrasting forms of one trait • one of these traits will not show in the first generation ...
Human Genetics - Esperanza High School
Human Genetics - Esperanza High School

... chromosome, may affect one of every two newly fertilized eggs • Polyploidy = three or more of each chromosome, is common in plants but is lethal to the zygote if it occurs in humans ...
Chapter 31
Chapter 31

... The length of the inactive region varies from cell to cell. o As a result, inactivation of genes in this vicinity causes position effect variegation. Similar spreading effects occur at telomeres and at the silent cassettes in yeast mating type. ...
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Chapter 13 PowerPoint.ppt

... • Requires SRY gene on Y for “maleness” ...
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X-inactivation



X-inactivation (also called lyonization) is a process by which one of the two copies of the X chromosome present in female mammals is inactivated. The inactive X chromosome is silenced by its being packaged in such a way that it has a transcriptionally inactive structure called heterochromatin. As nearly all female mammals have two X chromosomes, X-inactivation prevents them from having twice as many X chromosome gene products as males, who only possess a single copy of the X chromosome (see dosage compensation). The choice of which X chromosome will be inactivated is random in placental mammals such as humans, but once an X chromosome is inactivated it will remain inactive throughout the lifetime of the cell and its descendants in the organism. Unlike the random X-inactivation in placental mammals, inactivation in marsupials applies exclusively to the paternally derived X chromosome.
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