|
Abdul-Latif, H; Leiberman, E; Brown, M R et al. (2000) Growth hormone deficiency type IB caused by cryptic splicing of the GH-1 gene. J Pediatr Endocrinol Metab 13:21-8
|
|
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
|
|
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
|
|
Parks, J S; Brown, M R; Faase, M E (1997) The spectrum of growth-hormone insensitivity. J Pediatr 131:S45-50
|
|
Baumbach, L; Schiavi, A; Bartlett, R et al. (1997) Clinical, biochemical, and molecular investigations of a genetic isolate of growth hormone insensitivity (Laron's syndrome). J Clin Endocrinol Metab 82:444-51
|
|
Parks, J S; Adess, M E; Brown, M R (1997) Genes regulating hypothalamic and pituitary development. Acta Paediatr Suppl 423:28-32
|
|
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
|
