Different kinds of muscular dystrophy

    • [DOC File]Final Exam Review - June, 2003 (Chapters 7 - 12)

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      The different forms of a gene are called alleles. ... (RRYy), how many different kinds of phenotypes are their offspring expected to show?2. ... Duchenne muscular dystrophy. A chromosome consists of many genes. What are all the chromosomes except the sex chromosomes called? autosomes.

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    • [DOC File]Module 10 - DEPED-LDN

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      A disease called muscular dystrophy interrupts muscles and nerves acting together. Muscular dystrophy is the slow wasting away of muscle tissue. People with this disease may lose the use of some or all of their skeletal muscles. Although the cause of the disease is not exactly known, nerve cells leading to muscles are thought to cause the problem.

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    • [DOC File]Meiosis - Amok Science

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      Duchenne Muscular Dystrophy. Sample Sex-linked Trait Problems. In humans, red-green colorblindness is a recessive sex-linked trait. It is found on the X chromosome, not the Y. Because, males only have one X chromosome, they have a much greater chance of having red-green colorblindness.

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    • [DOC File]HL IB Biology I – Data Analysis #1 - Weebly

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      Herbicides are classified by the kinds of plants they kill and their mechanism of action. Broad-spectrum herbicides kill many different kinds of plants, but often kill the crop plant as well. ... In humans, Duchenne Muscular Dystrophy (DMD) is a lethal X-linked recessive disorder caused by mutations in the dystrophin gene. ... Different groups ...

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    • [DOC File]Sickle cell anemia presentation

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      Two different types of muscular dystrophy are caused by different types of mutations in the gene for a protein that helps to prevent muscle cells from dying prematurely. Duchenne muscular dystrophy is more severe.

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    • [DOC File]Chapter 15 Multiple Choice Practice - New Century Academy

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      a. It explains cases in which the gender of the parent from whom an allele is inherited affects the expression of that allele. b. It is greatest in females because of the larger maternal contribution of cytoplasm. c. It may explain the transmission of Duchenne muscular dystrophy. d.

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    • [DOCX File]Study Island - Ms. Doran's Biology Class - Home

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      A recessive gene located on the X chromosome is the cause of muscular dystrophy in affected individuals. Males are more likely to suffer from muscular dystrophy than females because ... different kinds of proteins.The proteins made by DNA have many jobs, such as acting as enzymes, storage, transport, and defense against diseases. 77. An . allele.

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    • [DOC File]Final Exam Review - June, 2003 (Chapters 7 - 12)

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      Duchenne muscular dystrophy. Three copies of chromsome 21 (Down’s Syndrome) is known as Trisomy 21. What chromosomes do people with Turner syndrome have? Only 1 X. Males with Klinefelter syndrome have an extra X chromosome (karyotype 47,XXY). Sickle cell anemia is a disorder that involves codominant alleles and it results in production

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    • [DOCX File]CourseSource

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      Muscular Dystrophy (MD) is a group of diseases that cause progressive weakness and loss of muscle mass. In MD, abnormal genes (mutations) interfere with the production of proteins needed to form healthy muscle. There are many different kinds of MD. Symptoms of the most common variety begin in childhood, primarily in boys.

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