Word Finder - mutation

definition

Any alteration or change.

definition

Any heritable change of the base-pair sequence of genetic material.

definition

A mutant.

definition

An alteration a particular sound of a word, especially the initial consonant, which is triggered by the word's morphological or syntactic context and not by its phonological context.

definition

A group of thrushes.

There's never been a mutation like this in the history of our people.

We need to know how many people have this mutation and where they are, Kris ordered.

As then the Ent is one, invariable and immutable, all plurality, variety and mutation belong to the Nonent.

Charcoal is a recessive mutation in need of preservation !

If it's hereditary, then the mutation has been hidden from us for, like, maybe even hundreds of thousands of years.

This change is called the " soft mutation."

These phenotypic variations have been shown to relate to the specific mutation generated, to environmental influences and to independently segregating modifier genes.

An accident or mutation in genetic development may also cause retardation.

With closed eyes, between sleeping and waking, many people see faces, landscapes and other things flash upon their view, pictures often brilliant, but of very brief duration and rapid mutation.

A better understanding of the factors that underlie variable penetrance in mutation carriers is needed to augment our ability to counsel individual women.

A point mutation is like a typo in the gene that causes it to work incorrectly.

Another study estimated that one in 4,000 females is affected by the full mutation.

This disorder is the result of a genetic mutation.

Therefore, once a mutation is found in one affected member, it is possible to test other members who may have symptoms or are at risk of developing CMT.

Testing during pregnancy to determine whether an unborn child is affected is possible if genetic testing in a family has identified a specific CMT-causing mutation.

The mutation was transmitted to later generations because people who carried a single copy of the mutated gene had a modified (but not abnormal) inflammatory response that may have protected them against some infectious agent at that time.

Fragile X syndrome is caused by a mutation in the FMR-1 gene, located on the X chromosome.

There is a 50 percent risk for a premutation carrier female for transmitting an abnormal mutation with each pregnancy.

A female's normal X chromosome may compensate for her chromosome with the fragile X gene mutation.

In studies of families into which infants with OI type II were born, most of the babies had a new dominant mutation in a collagen gene.

In an autosomal dominant pattern of inheritance, only one of these two copies needs to have the mutation (change) or defect in order for the child to have DM.

The specific mutation that causes DM1 is called a trinucleotide repeat expansion.

Some families with symptoms of DM do not have a mutation in the DMPK gene.

Instead, they have a mutation in a gene on chromosome 3 that causes four units within the gene to be repeated.

More than half of all girls with Turner syndrome are mosaics, which means that the mutation occurs in some but not all cells of their body.

Other members of the mother's family may also want to consider testing to find out if they carry the same gene mutation.

A small number of patients with PWS have a change (mutation) in the genetic material on the chromosome 15 inherited from their father.

More specialized DNA testing is required to detect maternal uniparental disomy or a mutation that disrupts imprinting.

This is because Rett's Disorder is caused by a genetic mutation.

The FMR1 gene can be passed from parent to child in a premutation form, which then may or may not fully mutate to cause Fragile X, or as a full mutation.

A father who carries the Fragile X mutation can only pass the milder, premutation form of the FMR1 gene to his daughters, even if he carries the full mutation gene.

Mothers who carry the altered gene can pass it to children of either sex, and can transmit the genetic condition in either the premutation or full mutation form.

Mothers who have one mutated X chromosome and one normal copy have a 50 percent chance of passing the mutation to each child they bear, though they are very likely to show no symptoms of fragile X themselves.

A simple blood test will reveal MECP2 mutation, but this mutation is also seen in other types of development disorders.

The severity of the condition, and the likely course the disease will take, is dependent on the location of the mutation and other factors.

It is estimated that 99.5 percent of the time, the mutation of the genes occurs sporadically.

Researchers also found that the missing DNA was present in the affected children's neurotypical parents, meaning the mutation is spontaneous and rarely passes directly from parent to child.

According to the National Institute of Neurological Disorders and Stroke, each of these conditions have a genetic component, whether a mutation of a single gene or more complicated vehicle for inheritance.

Rett's syndrome is the only pervasive developmental that has a known cause (MECP2 gene mutation).

While the brain differences associated with autism can't be traced back to a single gene mutation or difference, many researchers believe that genetics can play a role in developing the disorder.

Scientific experiments grafted Godzilla cells with her, and caused a mutation that included dinosaur like protrusions on the plant's surface.

This is exactly the nomenclature system laid down by Owen, Cope, Marsh and others, although established without any understanding of the law of mutation.

This change is called the " nasal mutation."

This change is called the " spirant mutation."

You might have an Immortal bloodline somewhere in your ancestry or a simple mutation.

The mutation started sometime after our births, Kris, Gabriel voiced.

Title The factor V Leiden mutation in Japanese couples with recurrent spontaneous abortion.

For years, breeders have used " mutation breeding " to develop new varieties.

Relatives of mutation carriers were genotyped in order to study the segregation of mutant alleles with obesity.

The same mutation of the tabby gene is now believed to produce the king cheetah 's coat.