1. Heterogenous growth hormone (GH) gene mutations in familial GH deficiency;Cogan;J Clin Endocrinol Metab,1993
2. Familial growth hormone deficiency: a model of dominant and recessive mutations affecting a monomeric protein;Cogan;J Clin Endocrinol Metab,1994
3. A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency - a clinical research center study;Cogan;J Clin Endocrinol Metab,1995
4. Screening for growth hormone (GH) gene splice-site mutations in sporadic cases with severe isolated GH deficiency using ectopic transcript analysis;Gerhard;J Clin Endocrinol Metab,1995
5. A novel mechanism of aberrant pre-mRNA splicing in humans;Cogan;Hum Mol Genet,1997