When a father and his two kids developed an array of peculiar symptoms, doctors, Brazilian researchers and the NIH partner

A patient’s genetic makeup and journey with leukemia highlights the need for more gene sequencing in minority children.

Living with a rare disease can be isolating, especially when doctors don’t know the condition exists in the first place.

U-M is looking for families with a child or children diagnosed with autism spectrum disorder to take part in a national study aimed at speed

Trained to interpret variations in your DNA, these specialists can help confirm a vision-related diagnosis and guide family members in gaugi