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The Journal of Endocrinology|August 1, 1977
Neonatal islet cell transplantation in the diabetic rat: effect on hepatic enzyme activity and glucose homeostasisY Mangnall, A Smythe, D N Slater, et al.
The Journal of Clinical Endocrinology and Metabolism|June 17, 1998
Pro239Ser: a novel recessive mutation of the Pit-1 gene in seven Middle Eastern children with growth hormone, prolactin, and thyrotropin deficiencyF Pernasetti, R D Milner, A A al Ashwal, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 1, 1994
Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patientM A Berg, R Peoples, L Pérez-Jurado, et al.
Pediatric Research|November 1, 1984
Reduced plasma somatomedin activity and costal cartilage sulfate incorporation activity during experimental growth retardation in the fetal ratF A De Prins, D J Hill, M Fekete, et al.
Journal of Medical Genetics|November 1, 1994
Genetic mapping of the FACC gene and linkage analysis in Fanconi anaemia familiesR A Gibson, D Ford, S Jansen, et al.
Archives of Disease in Childhood|August 1, 1987
United Kingdom multicentre clinical trial of somatremR D Milner, N D Barnes, J M Buckler, et al.
Clinical Endocrinology|July 1, 1979
Experience with human growth hormone in Great Britain: the report of the MRC Working PartyR D Milner, T Russell-Fraser, C G Brook, et al.
Human Mutation|January 1, 1996
Novel mutations and polymorphisms in the Fanconi anemia group C geneR A Gibson, N V Morgan, L H Goldstein, et al.
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