Matching Pairs Med Genetic 3Online version FOREIGN by Anthony Flish 1 Sex Reversal Syndrome 2 X-linked Recessive Pedigree 3 X-linked Dominant Pedigree 4 Hemophilia A or B is X-Linked recessive Disorder. Which lacks? 5 Autosomal Dominant inheritance 6 Y-linked 7 X-Linked Dominant inheritance 8 carrier frequency 9 Leber's Hereditary Optic Neuropathy, cause blindess, mitochondrial disease 10 p2+2pq+q2 and p+q=1 11 Autosomal Recessiv Inheritance 12 Autosomal Codominant Inheritance 13 Duchenne Muscular Dystrophy lacks Dystrophin which interact with actin as well as dystroglycan-sarcoglycan. stablizes sarcolemma 14 X-linked Recessive 15 Red-Green Color Blindess Mutated gene for NADH Dehydrogenase. No Father to Son transmission . Fragile X syndrome FMR1 protein. (CGG)-Arginine. lack light absorbing protein "Opsin" 2 alleles at locus produce 2 different phenotypes that appear in heterozygote (i.e. A,B,O blood group).. Emphysema (a1-antitrypsin) increase intracellular Ca2+, activation depend on protease. Kinase level in blood (20x). Clumsy. Becker Muscular Dystrophy is less severe. 2pq Hardy Weinberg Equation lacks clotting factor VIII or IX. -Tend to skip generation -affected offspring born to unaffected parents. -equal frequency between both sex. loss of SRY gene, gonad dysgenesis. affect both sex. appear in every generation. (CAN CAUSE NEW AUTOSOMAL DOMINANT MUTATION)
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