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  Home >> Genetics Dictionary >> Dominance - Dysplasia

Dominance (genetic)
An allele (A) is dominant if the phenotype of the heterozygote (Aa) is the same as the homozygote (AA). The allele (a) does not influence the heterozygote's phenotype and is called recessive. An allele may be partly, rather than fully, dominant; in that case, the heterozygous phenotype is nearer to, rather than identical with, the homozygote of the dominant allele.

Double Transformant
A bacteria that has simultaneously transformed two or more genes; the genes cotransformed are inferred to I closely linked because transforming DNA fragments are usually small.

Down Syndrome

A condition involving mental retardation due to the presence of an extra chromosome 21. Also called trisomy 21.  
2. A condition involving mental retardation and distinctive facial features which is due to an extra chromosome 21. This can be detected prenatally by chromosome  analysis on fetal cells obtained by amniocentesis.

Dominant
An allele that is almost always expressed, even if only one copy is present.
2. A characteristic of gene expression in which only one copy of a gene is needed in order for there to be manifestations of its presence.
3. The property of an allele where by possessing either one or
two copies of the allele results in the same phenotype. Contrast with recessive.

Dominant trait
A trait controlled by an allele that expresses itself even when heterozygous.

Dosage compensation
A mechanism by which the activity of a gene is increased or decreased depending on the number of copies of that gene present in the cell. Most commonly seen in genes found on the X chromosome, which must be regulated so that males and females have the same amount of gene product.

Double crossover
Two separate crossover events occurring within the same tetrad.
2. Breakage and interchange occurring twice within a tetrad involving two, three, or Jour of the chromatids.

Double helix
The twisted-ladder shape that two linear strands of DNA assume when complementary nucleotides on opposing strands bond together.

2. The structure of DNA proposed by Watson  and Crick, consisting of two antiparallel polynucleotid into a right-handed helix with approximately 10 base pairs per full turn of the double helix. 

3. The Watson-Crick model of DNA structure, involving coiling of two hydrogen-bonded polynucleotide, antiparallel strands wound into a right-handed spiral configuration.

Dysplasia
Abnormality of development of particular tissue types; alteration in size, shape, or organization of cells into tissue.

Draft Sequence
The sequence generated by the HGP as of June 2000 that, while incomplete, offers a virtual road map to an estimated 95% of all human genes. Draft sequence data are mostly in the form of 10,000 base pair-sized fragments whose approximate chromosomal locations are known. 

Duplication
The occurrence of a second copy of a particular of DNA. The duplicate sequence may appear next to the original or be copied elsewhere into the. genome. When the duplicated sequence is a gene, the event IS called gent. 2. The presence of an extra copy of chromosomal material.

Dysmorphic
Reflecting abnormality in morphological development; abnormality in the development of structure or form.

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