monosomies การใช้
- The most common abnormality is monosomy of chromosome 22.
- Turner's syndrome is also referred to as a monosomy X condition.
- Deletions of part of a chromosome cause partial monosomies, while duplications can cause partial trisomies.
- It is associated with other vascular anomalies, and some genetic syndromes such as monosomy X.
- Two studies found a rate of cardiovascular malformations of 30 % in a group of pure 45, X monosomy.
- An "'isochromosome "'is an unbalanced partial monosomy of the genes in the lost arm.
- Deletion of GPR35 gene may be responsible for brachydactyly mental retardation syndrome and is mutated in 2q37 monosomy and 2q37 deletion syndrome.
- Abnormalities in chromosomes such as trisomy 18, trisomy 13, and monosomy X have been shown to be tied to this disorder.
- "' 2q37 monosomy "'is a rare genetic disorder caused by a deletion of a segment at the end of chromosome 2.
- This results in the production of gametes which have either too many or too few of a particular chromosome, and is a common mechanism for trisomy or monosomy.
- In this case, the cell can be considered as carrying a monosomy for the chromosome on which the markers are located, or, possibly, as haploid.
- "' American Sign Language "': Because few individuals with Monosomy 1p36 develop complex speech, an alternate form of communication is critical to development.
- Monosomy is a form of aneuploidy with the presence of only one chromosome ( instead of the typical two in humans ) from a pair, which affects chromosome 14.
- The most accurate prognostic factor is molecular classification by Gene expression profiling outperforms all of the above-mentioned factors at predicting metastatic spread of the primary tumor, including monosomy 3.
- When 80 females with monosomy X were tested for measures of social cognition, the patients with a paternally derived X chromosome performed better than those with a maternally derived X chromosome.
- These changes include an extra copy of part of chromosome 7 in each cell ( partial trisomy 7 ) or a missing segment of the chromosome in each cell ( partial monosomy 7 ).
- The higher rate in the group of pure 45, X monosomy is primarily due to a difference in the rate of aortic valve abnormalities and coarctation of the aorta, the two most common cardiovascular malformations.
- Considering other karyotype groups, though, they reported a prevalence of 24.3 % and 11 % in people with mosaic X monosomy, and a rate of 11 % in people with X chromosomal structural abnormalities.
- As a result, the former cell gets three copies of the chromosome, a condition known as " trisomy ", and the latter will have only one copy, a condition known as " monosomy ".
- Upon examination, MDS-afflicted FA patients will show many clonal variations, appearing either prior or subsequent to the MDS . Furthermore, cells will show chromosomal aberrations, the most frequent being monosomy 7 and partial hematopoietic progenitor cell transplant is an option ).
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