Q3 2025 Earnings Call Transcript October 28, 2025 GeneDx Holdings Corp. misses on earnings expectations. Reported EPS is ...
Prevent is run by the Home Office and aims to stop terror attacks. Officials work with local authorities and community ...
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There were courageous medical staff at every crisis in life...Completion fee for the story contest o...
Hallym University Medical Center (Director Kim Yong-sun) successfully completed the '2025 Hallim University Medical Center ...
If you have ever welcomed a new baby into the world, you know the mix of hope and uncertainty that comes with those first days. For decades, newborn screening has been a quiet triumph of public health ...
A comprehensive eight-year study examining audiological outcomes of newborns screened for congenital cytomegalovirus (cCMV) ...
Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis and treatment, according to a new study. A baby's genome ...
Dr. Mary Erika Orteza, Medical Officer IV, Baguio General Hospital and Medical Center. BAGUIO CITY (PIA) — In line with the observance of Newborn Screening (NBS) Month this October and Newborn ...
Quantabio, announced the launch of the sparQ™ Lysis Kit. This product is the latest addition to the company’s comprehensive newborn screening workflow for sequencing dried blood spots. Quantabio will ...
Congenital cytomegalovirus (cCMV) is the most common infectious cause of birth defects and non-genetic hearing loss in the United States, yet it remains underdiagnosed due to the absence of universal ...
Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis and treatment, according to a new study. A baby’s genome ...
Jeanette Henriquez, on the left, stands with her two children, Jasmine Henriquez and Dominic Henriquez. Dominic Henriquez was diagnosed with Hunter Syndrome in 2011 before the condition was added to ...
Newborn babies in England will now be routinely screened for a rare genetic condition, NHS England has announced. Hereditary tyrosinaemia type 1 (HT1) affects around seven UK babies annually, causing ...
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