N C Fraser

A homozygous splice site mutation affecting the intracellular domain of the growth hormone (GH) receptor resulting in Laron syndrome with elevated GH-binding protein.

Kate Woods, N C Fraser, M C Postel-Vinay et al. · The Journal of Clinical Endocrinology & Metabolism · 1996 · 123 citations

Human Growth, Genetics, Molecular Genetics +18

Clonidine is a better test for growth hormone deficiency than insulin hypoglycaemia.

N C Fraser, J. Seth, N. S. BROWN · Archives of Disease in Childhood · 1983 · 47 citations · Full text

Growth Hormone, Short Stature, Human Growth +11

Accidental poisoning deaths in British children 1958-77.

N C Fraser · BMJ · 1980 · 37 citations · Full text

Safety Packaging, Pharmacotherapy, Injury Prevention +20

A boy with coeliac disease and obesity

Olumuyiwa Oso, N C Fraser · Acta Paediatrica · 2006 · 19 citations

Bone density and body composition in children with growth hormone insensitivity syndrome receiving recombinant IGF‐I

N. Shaw, N C Fraser, S Rose et al. · Clinical Endocrinology · 2003 · 17 citations