Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK046312-03
Application #
2145498
Study Section
Endocrinology Study Section (END)
Project Start
1994-01-01
Project End
1997-12-31
Budget Start
1996-05-01
Budget End
1997-12-31
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Name
Emory University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
042250712
City
Atlanta
State
GA
Country
United States
Zip Code
30322
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Arnhold, I J; Nery, M; Brown, M R et al. (1998) Clinical and molecular characterization of a Brazilian patient with Pit-1 deficiency. J Pediatr Endocrinol Metab 11:623-30
Wu, W; Cogan, J D; Pfaffle, R W et al. (1998) Mutations in PROP1 cause familial combined pituitary hormone deficiency. Nat Genet 18:147-9
Brown, M R; Parks, J S; Adess, M E et al. (1998) Central hypothyroidism reveals compound heterozygous mutations in the Pit-1 gene. Horm Res 49:98-102
Parks, J S; Brown, M R; Faase, M E (1997) The spectrum of growth-hormone insensitivity. J Pediatr 131:S45-50
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Binder, G; Brown, M; Parks, J S (1996) Mechanisms responsible for dominant expression of human growth hormone gene mutations. J Clin Endocrinol Metab 81:4047-50
Binder, G; Ranke, M B (1995) Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis. J Clin Endocrinol Metab 80:1247-52