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