Smith Family Clinic for Genomic Medicine and HudsonAlpha were recently featured in a special edition of Rare Revolution Magazine. Rare Revolution is a UK-based digital magazine giving a voice to patients affected by rare conditions and the charities that represent and support them. The September edition focused on genomics, clinical trials and rare disease […]
Clinic Medical Director David Bick, MD, sat down with Clinical OMICs magazine to discuss the use of next-generation sequencing (NGS) for the identification and treatment of rare disease. “We are rapidly reaching the point where we do whole genome sequencing on anybody you think has a rare disease,” said Bick. Read the full story on page […]
Huntsville, Ala. – HudsonAlpha Institute for Biotechnology is giving patients a chance at finding a diagnosis with the Hero Fund. Established by an anonymous donation to the HudsonAlpha Foundation, the Hero Fund helps patients at Smith Family Clinic for Genomic Medicine who need, but cannot afford, access to genomic medicine. Smith Family Clinic, powered by HudsonAlpha, […]
HudsonAlpha and Smith Family Clinic genetic counselors attended the NORD Rare Disease Breakthrough Summit Oct. 17-18. The Rare Disease Report caught up with Meagan Cochran to discuss whole genome sequencing at the Clinic.
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The Smith Family Clinic for Genomic Medicine in Huntsville Alabama has been established to use the power of genomics to solve undiagnosed and misdiagnosed cases and provide answers to families and physicians. The clinic’s mission is to provide the best positive medical experience and the information to make future health care decisions.
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