Published on
Breaking Through with Madeline Bell’s “Pioneered at CHOP” series highlights stories about some of CHOP’s amazing breakthroughs, told by the people who made them.
Published on
Learn more about Children’s Hospital of Philadelphia's efforts to define the underlying genetic etiologies of CDH to better understand why CDH occurs and how it can be more effectively treated.
Published on
The Kabuki Syndrome Clinic is one of the few of its kind in the world and offers a multidisciplinary team approach to treat patients with this rare genetic condition.
Published on
Children’s Hospital of Philadelphia was named one of the 15 most innovative children’s hospitals by Parents magazine based on the results of a comprehensive survey.
Published on
Roberts Individualized Medical Genetics Center Outlines Framework for Centralized Approach to Genetic and Genomic Testing
Published on
A research collaboration that shares genetic data among pediatric hospitals has received a multi-year federal grant to scale up its network, aimed at advancing precision medicine for children.
Published on
Families from across the globe gather for a symposium about CHOPS syndrome — a rare genetic condition identified in 2015 by researchers at Children's Hospital of Philadelphia.
Published on
Proton therapy at CHOP helped Elena regain her vision and remain free of craniopharyngioma two years after treatment.
Published on
Aileen and Brian Roberts' commitment to Dr. Levine’s research into the genetic causes of hypoparathyroidism in children can be life changing.
Published on
Genetic counselor Emma Bedoukian, MS, LCGC, guides patient families as they uncover answers to their child's medical mystery. This is a day in her life.