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Yet, the degree of mosaicism does not determine response to drug treatment.
This may not be the case as the incidence of mosaicism is often relatively high.
This type of mosaicism is most often associated with normal pregnancy outcome.
It has been confirmed that the disorder is an example of genetic mosaicism.
The presence of mosaicism is estimated to be relatively common in affected individuals (67-90%).
People who have mosaicism are often called chimeras but this is a mistake.
Generally 20 cells are analyzed which is enough to rule out mosaicism to an acceptable level.
This type of mosaicism is more commonly associated with delayed growth in the fetus.
However, they may do so due to mosaicism.
Parents may either be clinically affected or have germline mosaicism.
Patients with Turner's mosaicism can reach normal average height.
The full range of ambiguity of structure may occur, especially if mosaicism is present.
Mosaicism also results from a phenomenon known as X-inactivation.
The most common cause of mosaicism in mammalian females is X-inactivation.
Germline mosaicism has been suggested for several families with multiple affected siblings.
Trisomy 8 mosaicism is less severe and individuals with this condition are more likely to survive.
The most common form of mosaicism found through prenatal diagnosis involves trisomies.
The stripes are a type of genetic mosaicism.
It is, presumably, a rare cutaneous form of mosaicism.
This is an example of mosaicism or chimerism.
Mitotic nondisjunction after conception would lead to mosaicism, and is discussed later.
Mosaicism occurs in about 30 percent of embryos.
On this page, only genetic mosaicism is discussed.
In some affected individuals, only a percentage of cells may contain the chromosomal condition (mosaicism).
This phenomenon is known as mosaicism or chimerism.