1. Allgrove J. et al. Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production. Lancet 8077:1284, 1978.

2. Arai K, Chrousos GP. Syndromes of glucocorticoid and mineralocorticoid resistance. Steroids 60:173, 1995.

3. Bichet DG. Nephrogenic diabets insipidus. Am J Med 105:431, 1998.

4. Bolander FF. Molecular Endocrinology. San Diego: Academic Press, Inc., 1989. P. 78.

5. Clark AJ, et al. Familial glucocorticoid deficiency: one syndrome, but more than one gene. J Mol Med 75:394, 1997.

6. Dufau ML. The luteinizing hormone receptor. Annu Rev Physiol 60:461, 1998.

7. Feldman D, Malloy PJ. Hereditary 1 ,25-dihydroxyvitamin D- resistant rickets Molecular basis and implications for the role of 1,25(OH)2D3 in normal physiology. Mol Cell Endocrinol 72:C57- C62, 1990.

8. Geffner ME, Golde DW. Selective insulin action on skin, ovary, and heart in insulin-resistant states. Diabetes Care 11:500, 1988.

9. Gelbert L, et al. Chromosomal localization of the parathyroid hor- mone/parathyroid hormone-related protein receptor gene to human chromosome 3p21.1-p24.2. J Clin Endocrinol Metab 79:1046, 1994.

10. LeRoith D, et al. Insulinlike growth factors and their receptors as growth regulators in normal physiology and pathologic states. Trends Endocri-nol Metab 2:134, 1991.

11 . McKusick VA. Mapping the genes for hormones and growth factors and the mutations causing disorders of growth. Growth Genet Horm 5:1, 1989.

12. Michell RH. Post-receptor signalling pathways. Lancet 1:765, 1989.

13. Okusa MD, Bia MJ. Bartter's syndrome. In MP Cohen, PP Foa (eds), Hormone resistance and other endocrine paradoxes. New York: Springer, 1987. Pp. 231.

14. Stavrou SS, et al. A novel mutation of the human luteinizing hormone re-ceptor in 46XY and 46XX sisters. J Clin Endocrinol Metab 83:2091, 1998.

15. Taylor SI. Molecular mechanisms of insulin resistance: Lesson from pa-tients with mutations in the insulin receptor gene. Diabetes 41 : 1473, 1992.

16. Theriault A, et al. Regional chromosomal assignment of the human glu-cocorticoid receptor gene to 5q31. Hum Genet 83:289, 1989.

17. Tsai-Morris CH, et al. A novel human luteinizing hormone receptor gene. J Clin Endocrinol Metab 83:288, 1998.

18. Usala SJ, Weintraub BD. Thyroid hormone resistance syndromes. Trends Endocrinol Metab 2:140, 1991.

19. Usdin , et al. Assignment of the human PTH2 receptor gene (PTHR2) to chromosome 2q33 by fluorescence in situ hybridization. Genomics 37:140, 1996.

20. Van Dop C. Pseudohypoparathyroidism: Clinical and molecular aspects. SeminNephrol9:168, 1989.

21 . Wu SM, et al. Genetic heterogeneity of adrenocorticotropin (ACTH) re-sistance syndromes: identification of a novel mutation of the ACTH re-ceptor gene in hereditary glucocorticoid deficiency. Mol Genet Metab 64:256, 1998.