Loading...
Keywords
Last Name
Institution

Search Results (25)

Click the Why column to see why an item matched the search.

MatchTypeWhy
Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts.Academic Article Why?
Congenital H-type tracheoesophageal fistula: A multicenter review of outcomes in a rare disease.Academic Article Why?
Expediting rare disease diagnosis: a call to bridge the gap between clinical and functional genomics.Academic Article Why?
Sources of unease about the use of genome sequencing for diagnosing rare diseases in children.Academic Article Why?
Rare DiseasesConcept Why?
Reverse Translation in Advancing Pharmacotherapy in Pediatric Rheumatology: A Logical Approach in Rare Diseases with Limited Resources.Academic Article Why?
Vivian, JayPerson Why?
Smail, CraigPerson Why?
Adopting orphans: comprehensive genetic testing of Mendelian diseases of childhood by next-generation sequencing.Academic Article Why?
Dangerous and expensive screening and treatment for rare childhood diseases: the case of Krabbe disease.Academic Article Why?
Gannon, JenniferPerson Why?
Sharma, MuktaPerson Why?
Younger, ScottPerson Why?
Lantos, JohnPerson Why?
Proceedings of the 2019 Santa Fe Bone Symposium: New Concepts in the Care of Osteoporosis and Rare Bone Diseases.Academic Article Why?
Per Page    Page  of 2last Nextnext
Prev
Search Criteria
  • Rare Disease
Filter by Type