K. Woods

Clinical and Endocrine Characteristics in Atypical and Classical Growth Hormone Insensitivity Syndrome

M. Preece, M. Savage, P. Crock, 2001, Hormone Research in Paediatrics.

Growth Hormone Insensitivity

S. Amselem, M. Savage, A. Clark, 2004 .

Defects of the growth hormonereceptor and their clinical implications

S. Amselem, M. Savage, A. Clark, 1999 .

Defects of the growth hormone receptor and their clinical implications.

S. Amselem, M. Savage, A. Clark, 1999, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

Genetic linkage of Werner's syndrome to five markers on chromosome 8

D. Drayna, M. Goto, K. Woods, 1992, Nature.

Relationship of endocrinopathy to iron chelation status in young patients with thalassaemia major.

M. Savage, R. Grundy, J. Evans, 1994, Archives of disease in childhood.

Association of the INS VNTR with size at birth

J. Todd, S. Ring, M. Pembrey, 1998, Nature Genetics.

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

M. Polymeropoulos, T. Meitinger, T. Strom, 2000, Nature Genetics.

Early growth is not increased in untreated moderately severe 21‐hydroxylase deficiency

A. Wedell, E. Ritzén, K. Woods, 1995, Acta paediatrica.

Laron syndrome: typical and atypical forms.

M. Savage, K. Woods, 1996, Bailliere's clinical endocrinology and metabolism.

Mutations in a new gene in Ellis-van Creveld syndrome and Weyers acrodental dysostosis

M. Polymeropoulos, T. Meitinger, T. Strom, 2000, Nature Genetics.