The Power of an Undiagnosed Diseases Program in a Clinical Research Enterprise

Principles and Practice of Clinical Research

Volumn , Issue , 2012, Pages 701-705

  Gahl, William A ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84884429124     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-12-382167-6.00048-5     Document Type: Chapter

References (3)

1. St Hilaire C., Ziegler S.G., Markello T., Brusco A., Groden C., Gill F., et al. NT5E mutations and arterial calcifications. N Eng J Med 2011, 364:432-442.
2. The Metabolic and Molecular Bases of Inherited Disease 2001, McGraw-Hill, New York, c. 199, pp. 5085-108. 8th ed. C.R. Scriver, A.L. Beaudet, W.S. Sly, D. Valle, B. Vogelstein (Eds.).
3. Moore B., Hu H., Singleton M., Reese M.G., De La Vega F.M., Yandell M. Global analysis of disease-related DNA sequence variation in 10 healthy individuals: implications for whole genome-based clinical diagnostics. Genet Med 2011, 13(3):210-217.