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