Examples of 'uniparental' in a sentence

Meaning of "uniparental"

uniparental (adjective) - Refers to something derived from or relating to a single parent, often used in genetics to describe inheritance from only one parent
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  • From or with only one parent.

How to use "uniparental" in a sentence

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uniparental
It can also be associated with uniparental isodisomy.
Uniparental inheritance of imprinted genes can also result in phenotypical anomalies.
This phenomenon is called maternal uniparental disomy.
Uniparental care species are also rare at higher latitudes and more common nearer the equator.
This approach could be used to detect uniparental disomy.
The revealed peculiarities in the uniparental markers are a legacy of the Finnish population history.
This is referred to as maternal uniparental disomy.
Uniparental DNA analysis has established ties between Berbers and other Afroasiatic speakers in Africa.
This is known as uniparental disomy.
Consult your physician or genetic counselor for more information regarding uniparental disomies.
Animation of uniparental isodisomy.
This uniparental inheritance is an example of non-Mendelian inheritance.
Detailed information on uniparental disomy.
Uniparental reproduction may also occur by apomixis, an asexual process.
It is always uniparental.

See also

Uniparental lineage, Inheritance received from only one of the parents.
Correns proposed that leaf color in Mirabilis was passed on via a uniparental mode of inheritance.
Genomic imprinting and uniparental disomy, however, may affect inheritance patterns.
This phenomenon is called paternal uniparental disomy UPD.
Uniparental paternal disomy in Angelman's syndrome.
Genetic instability, to include uniparental disomy.
Why is uniparental disomy a problem?
So you end up with what 's known as uniparental disomy.
Uniparental disomy of 7.
If both of the retained chromosomes come from the same parent, then uniparental disomy results.
This system is named DUI ( doubly uniparental inheritance ) and is exclusive to bivalves.
For an example, please see What are genomic imprinting and uniparental disomy?
Other, less common mechanisms include uniparental disomy, sporadic mutations, chromosome translocations, and gene deletions.
CMA testing revealed absence of heterozygosity spanning the entire chromosome 15, suggesting uniparental isodisomy 15.
Maternal uniparental disomy of chromosome 7 is observed in 10 % of patients.
This condition is called paternal uniparental disomy ( UPD ).
This is known as uniparental disomy ( UPD ).
In 10 % of the cases the syndrome is associated with maternal uniparental disomy ( UPD ) on chromosome 7.
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15.

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