L. Rees

Frasier syndrome, part of the Denys Drash continuum or simply a WT1 gene associated disorder of intersex and nephropathy?

P. Scambler, P. Hindmarsh, E. Charmandari, 2000, Clinical endocrinology.

INCREASED PRODUCTION OF α‐MELANOCYTE‐STIMULATING HORMONE IN THE PITUITARY GLAND OF PATIENTS WITH UNTREATED ADDISON'S DISEASE

P. Coates, A. Mcnicol, I. Doniach, 1988 .

Microcephaly, focal segmental glomerulonephritis and marfanoid habitus in two sibs.

R. Houlston, K. Macdermot, J. Slack, 1992, Clinical dysmorphology.

A stable, nonsense mutation associated with a case of infantile onset polycystic kidney disease 1 (PKD1).

P. Harris, J. L. San Millán, A. Ong, 1996, Human molecular genetics.

A CASE OF PITUITARY DEPENDENT CUSHING'S DISEASE WITH CLINICAL AND BIOCHEMICAL FEATURES OF THE ECTOPIC ACTH SYNDROME

J. B. Millar, J. Pickard, J. Pickard, 1985, Clinical endocrinology.