Significats de genetic condition en anglès

Autism is a heterogeneous disorder that can reveal a specific genetic disease.

Cancer is a genetic disease resulting from germline or somatic genetic aberrations.

Sharon Bernardi lost all seven of her children to a rare genetic disease.

This finding may contribute to clinical treatment of genetic disease or tissue repair.

The best-fit genetic disease model for this marker is a recessive genetic model.

I have xeroderma pigmentosum-XPfor short- arareand frequently fatal genetic disorder.

This is a genetic disorder that most people have never heard of.

Beta-thalassemia is a genetic disorder caused by mutations in the beta-globin gene.

Are these advantages as important as removing a genetic disorder from my genome?

Let's pretend I carry the gene responsible for a genetic disorder.

Mutations responsible for inherited disease may act by disrupting normal transcriptional splicing.

Cystic fibrosis is the most common life-threatening inherited disease in Ireland.

Cystic fibrosis is Ireland's most common life-threatening genetically inherited disease.

So Tessie Wartliz was suffering from an inherited disease commonly called "Greed."

Fanconi anemia (FA) is a recessive inherited disease characterized by defective DNA repair.

This had been a vow taken by him and his siblings in an effort to end generations of familial disorder.

Cobalamin C is a rare inborn disorder of metabolism that results in multisystemic abnormalities, including progressive visual deficits.

I want to know if it could have been a hereditary disease.

A low origin is like an hereditary disease-itwill bear no strain.

Some terrible hereditary disease, are we planning a trip to the moon?

I will refrain, for instance, from bringing up the subject of hereditary disease.

Medical Matters: Medicine, like politics, can be a hereditary disease.

Interestingly, the latest advances in AMD research also highlight common molecular disease pathways with other neurodegenerative disorders.

Thus, there is a high clinical need for molecular disease biomarkers to aid in differentiating these distinct phenotypes.

These cells remain after IM therapy, even when apparently complete responses are achieved, and they probably explain molecular disease persistence.

These patients are typically younger and suffer from conditions caused by a known molecular disease mechanism and a peculiar sarcopenic phenotype.

Fluorogenic probes that signal the presence of specific DNA or RNA sequences are key enabling tools for molecular disease diagnosis and imaging studies.

These transcription units represent candidate genes for multiple hereditary diseases, including HPC1.

Works with family trees and illnesses, Icelandic families and hereditary diseases, genetic diseases.

They are peculiarly indicative of hereditary diseases, especially lungs, heart, nerves, and spine.

Prevalence: Alpha-1 antitrypsin deficiency is one of the most common hereditary diseases in Caucasians of European descent.

I don't know about any hereditary diseases.