Four out of the six members of the Jahnz family have a blood clotting disorder called protein S deficiency. Staying positive has been a huge
We asked Dr. Joseph Lillegard, director of research and open fetal surgery, a few questions about his dedicated work in genomics.
Learn more about the Koch family’s experience with the genomic medicine program at Children’s Minnesota.
$2.3 million was raised at Star Gala 2019 to support the genomic medicine program at Children’s Minnesota.
The 28th annual Star Gala brought more than 900 people to The Depot in Minneapolis and raised a record breaking $2.3 million of vital funds
Annie Waters, vice president of foundation operations, and youth committee members J.J. Harrington and Lauren Smith discussed Children’s genomic medicine program and how to support
The genomics team at Children’s diagnosed a patient with a rare disease: Generalized Arterial Calcification of Infancy.
At just 6 years old, Anna has overcome more than most people ever will. But despite her rare chromosomal abnormality, Anna won’t be slowed down.
The Star Tribune spoke with Dr. Nancy Mendelsohn, chief of specialty pediatrics, about Children’s Minnesota’s participation in the Sanford Children’s Genomic Medicine Consortium.
Reach us 24/7 for patient referrals, consults, admissions and neonatal transport.
© 2024 Children’s Minnesota
Children’s Minnesota is registered as a 501(c)(3) non-profit organization. Our tax identification number is 41-1754276.
