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Androgen Insensitivity Syndrome - Home

DNA Sequence and DNA Motifs. Phylogeny ligand binding domain. Conclusions and future directions. This web page was produced as an assignment for Genetics. An undergraduate course at UW-Madison. Figure 1 Inheritance pattern of an X-linked, recessive allele. Figure 2 A family tree of female carrier of AIS, her brother and sons with completely penetrant AIS. Androgen Insensitivity Syndrome AIS. AIS occurs in approximately 1 in 20,000 births and is the most common male pseudohermaphroditism 1. Cause.
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Androgen Insensitivity Syndrome - Home

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DNA Sequence and DNA Motifs. Phylogeny ligand binding domain. Conclusions and future directions. This web page was produced as an assignment for Genetics. An undergraduate course at UW-Madison. Figure 1 Inheritance pattern of an X-linked, recessive allele. Figure 2 A family tree of female carrier of AIS, her brother and sons with completely penetrant AIS. Androgen Insensitivity Syndrome AIS. AIS occurs in approximately 1 in 20,000 births and is the most common male pseudohermaphroditism 1. Cause.

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This website trammellgen677s09.weebly.com states the following, "This web page was produced as an assignment for Genetics." Our analyzers viewed that the website said " An undergraduate course at UW-Madison." The Website also said " Figure 1 Inheritance pattern of an X-linked, recessive allele. Figure 2 A family tree of female carrier of AIS, her brother and sons with completely penetrant AIS. AIS occurs in approximately 1 in 20,000 births and is the most common male pseudohermaphroditism 1."

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