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 ...
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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 ...
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News Medical on MSNDiscovering a clue to what causes reproductive complicationsOur 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, ...
Birth defects: A leading cause of infant mortality Birth defects affect 3% of pregnancies in the U.S. They can be caused by exposures to certain medications, infections, maternal diseases or genetics.
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 ...
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News Medical on MSNScientists uncover hidden genetic causes of congenital heart diseaseScientists 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.
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