Примери за използване на Parents are carriers на Английски и техните преводи на Български
{-}
-
Colloquial
-
Official
-
Medicine
-
Ecclesiastic
-
Ecclesiastic
-
Computer
If both parents are carriers, they….
Cystic fibrosis gets passed down if both parents are carriers.
And if both parents are carriers of similar sites?
It is genetic and recessively inherited which means both parents are carriers.
If you have JEB, both your parents are carriers of the mutated gene but they do not have symptoms.
These odds are the same for each pregnancy when both parents are carriers.
In the dominant form, both parents are carriers of the mutated gene, with neither dog showing symptoms.
One of its peculiarities is that it only takes place when the two parents are carriers.
The condition occurs when both parents are carriers for thalassemia.
But, if both parents are carriers, the chances of passing the disorder on is much higher.
TSD is an autosomal recessive genetic disorder,meaning that when both parents are carriers, there is a 25% risk of giving birth to an affected child.
Both parents are carriers(a carrier has only one mutated copy but not the disease) and not patients.
If both parents are carriers, the child will have a 25% chance of inheriting both copies of the mutation, thus leading to the development of the genetic disease.
Parents are carriers of the flawed gene and it can lurk undetected for generations, suddenly emerging when an unlucky combination gives a child two copies of it.
The parents are carriers: As shown below, the father is blue and mother is yellow, they contribute to two possible alleles(r or R) of MC1R variants to their baby.
However, as mentioned above,the risk of having a baby with PKU will only appear if both parent are carriers of the pathological gene.
The parents are all carriers of the anomaly.
This means that both parents are healthy carriers of a mutated gene.
Hence, both parents are healthy carriers(a carrier has only one mutated copy but not the disease).
Hence, both parents are generally carriers(a carrier has only one mutated copy but not the disease) and not patients.
Hence, both parents are generally carriers(a carrier has only one mutated copy but not the disease) and not patients.
Most often, PKU is passed to children by two parents who are carriers of the disorder, but don't know it.
Parents often don't find out they are carriers of these diseases until they give birth to sick children.
First of all, those future parents, whose blood tests reliably confirmed that parents are both carriers of serious genetic diseases.
DNA testing is available to help parents and siblings determine if they are carriers of this type of gene mutation.
The most common congenital dysfunction of the cortexadrenal gland arises if the disease was detected at least one of the parents, or if the parents are direct carriers of the gene responsible for the transit of proteins that are needed to produce hormones of the adrenal cortex.
To have the disease, both parents must be carriers.
For the disease to be passed on, both parents must be carriers.
In order to get this disease, both parents must be carriers.