chromosomal translocation

A novel chromosomal translocation causing the syndrome was described in 2007.

The Robo1 protein is thought to be associated with dyslexia, possibly through chromosomal translocation.

Thus, chromosomal translocation is a main cause of hermaphroditism.

They are a type of chromosomal translocation.

The most common is a chromosomal translocation involving the nucleophosmin gene on chromosome 5.

It is a type of myeloproliferative disease associated with a characteristic chromosomal translocation called the Philadelphia chromosome.

Chromosomal translocation and extra chromosomes help create abnormally high activity of certain proto-oncogenes.

These phenotypes are often due to a chromosomal translocation such that the color gene is now close to a region of heterochromatin.

It should not be confused with chromosomal translocation, which is rearrangement of parts between non-homologous chromosomes.

The other 20% of cases are caused by a familial chromosomal rearrangement called chromosomal translocation.

A chromosomal translocation (another type of chromosome abnormality)

Tissue cytogenetics - the visualization of chromosomes to identify genetics defects such as chromosomal translocation.

In humans it is located on chromosome 1, at the breakpoint associated with the chromosomal translocation found in Schizophrenia.

Morphologic and immunohistochemical findings are corroborated with an associated chromosomal translocation, of which there are several.

Overexpression can happen in one of three ways: as a result of gene amplification, impaired protein degradation, or chromosomal translocation.

Mutations associated with papillary thyroid cancer are mainly two forms of chromosomal translocation and one form of point mutation.

Uses: Chromosomal translocation MRD detection is widely used as a standard clinical practice.

Chromosomal translocation occurs when two separate chromosomal regions become abnormally fused, often at a characteristic location.

Possessing chromosomes of varying shapes is generally the result of a chromosomal translocation or chromosomal inversion.

CML was the first malignancy to be linked to a clear genetic abnormality, the chromosomal translocation known as the Philadelphia chromosome.

Although the chromosomal translocation involving RARα is believed to be the initiating event, additional mutations are required for the development of leukemia.

The 2;5 chromosomal translocation is associated with approximately 60% anaplastic large-cell lymphomas (ALCLs).

TEL-JAK2 is a gene fusion resulting from a chromosomal translocation between chromosomes 9 and 12 observed in human leukemia.

Diagnosis of synovial sarcoma is made by immunohistochemical analysis, ultrastructural findings, and demonstration of the specific chromosomal translocation t(x;18)(p11.2;q11.2).

These include the addition of chromosomes, the loss of entire chromosomes, partial loss of chromosomes and chromosomal translocation.