monosomy मीनिंग इन हिंदी

अधिक: आगे

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.

संज्ञा.

chromosomal abnormality consisting of the absence of one chromosome from the normal diploid number