Scientists have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.

"Our research reveals the potential for digenic inheritance—where two genes work together to cause disease—expanding our ...

“Now we have a cell with a wrong chromosome.” “This becomes a major source of birth defects, cancer or even infertility. Why does this all happen? Well, that takes us back to square ...

These findings highlight the need for high-resolution genetic screening in children with CHD and additional birth defects, even if they have had a normal karyotype. Our results indicate that a ...

Omfalokel adalah cacat lahir pada perut janin. Berikut adalah penjelasan tentang tanda, penyebab, hingga cara mencegahnya.

Our cells constantly receive DNA damage from factors such as ultraviolet rays, irradiations, toxins and chemicals. For women, ...

Prenatal genetic screening is commonly used to identify pregnancies at high risk for birth defects, including neural tube defects and genetic conditions such as Down syndrome. In contrast to other ...

Our cells constantly receive DNA damage from factors such as ultraviolet rays, irradiations, toxins and chemicals. For women, ...

Preimplantation Genetic Testing for Aneuploidies (PGT ... The role of PGT-A in preventing birth defects Dr Ritu Hinduja revealed, “PGT-A is a pioneering assisted reproduction device that ...

Scientists at the Icahn School of Medicine at Mount Sinai and collaborators have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.