heterozygous genotype

См. также в других словарях:

• Genotype — For a non technical introduction to the topic, see Introduction to genetics. Here the relation between genotype and phenotype is illustrated, using a Punnett square, for the character of petal colour in pea. The letters B and b represent genes… …   Wikipedia

• Heterozygous — The state of having two different forms of a particular gene, one inherited from each parent. A person who is heterozygous is called a heterozygote or a gene carrier. For example, a woman who is heterozygous for cystic fibrosis (CF) carries the… …   Medical dictionary

• evolution — evolutional, adj. evolutionally, adv. /ev euh looh sheuhn/ or, esp. Brit., /ee veuh /, n. 1. any process of formation or growth; development: the evolution of a language; the evolution of the airplane. 2. a product of such development; something… …   Universalium

• Dominance (genetics) — For other uses, see Dominance. A pedigree chart shows how genes are inherited. Dominance in genetics is a relationship between two variant forms (alleles) of a single gene, in which one allele masks the effect of the other in influencing some… …   Wikipedia

• Cat body type genetic mutations — Cats, like all living organisms, occasionally have mutations that affect their body type. Sometimes, these changes in body type are striking enough that humans select for and perpetuate them. This is not always in the best interests of the cat,… …   Wikipedia

• Hybrid (biology) — In biology and specifically, genetics, the term hybrid has several meanings, all referring to the offspring of sexual reproduction.[1] In general usage, hybrid is synonymous with heterozygous: any offspring resulting from the mating of two… …   Wikipedia

• CLN3 — Ceroid lipofuscinosis, neuronal 3 Identifiers Symbols CLN3; BTS; JNCL; MGC102840 External IDs …   Wikipedia

• HLA-DQ6 — heteroisoform isoformgroup = HLA DQ6 polymer type = MHC Class II, DQ cell surface antigen image source = Illustration of HLA DQ with bound peptide isoformCount = 4 subunit1 = DQA1 subunit2 = DQB1 isoform1 = DQ α1.3β6.1 nick1 = DQ6.1 allele1a =… …   Wikipedia

• familial hypercholesterolemia — Pathol. an inherited metabolic disorder caused by a lack or malfunction of receptors for the low density lipoproteins that activate removal of cholesterol from the blood. Abbr.: FH. * * * ▪ medical disorder  an inherited metabolic disease that is …   Universalium

• Codominance — refers to a relationship between two alleles of a gene. It occurs when the contributions of both alleles at a single locus are visible and do not overpower each other in the phenotype. For instance, in the ABO system, the IA and IB alleles are co …   Wikipedia

• heredity — /heuh red i tee/, n., pl. heredities. Biol. 1. the transmission of genetic characters from parents to offspring: it is dependent upon the segregation and recombination of genes during meiosis and fertilization and results in the genesis of a new… …   Universalium