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American Journal of Human Genetics|May 23, 1998
Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafnessL M Moynihan, S E Bundey, D Heath, et al.
Acta Astronautica|July 1, 1994
Systems integration in space flight environmental risk managementG W Morgenthaler, J R Schulz, R N Eberhardt, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|April 22, 2005
Childhood diabetes presenting with hyperosmolar dehydration but without ketoacidosis: a report of three casesM J R Kershaw, T Newton, T G Barrett, et al.
Archives of Disease in Childhood|October 8, 2008
Management and 1 year outcome for UK children with type 2 diabetesJ P H Shield, R Lynn, K C Wan, et al.
Acta Paediatrica (Oslo, Norway : 1992)|September 24, 2004
Wolcott-Rallison syndrome: a clinical and genetic study of three children, novel mutation in EIF2AK3 and a review of the literatureS Iyer, M Korada, L Rainbow, et al.
The Journal of Pediatrics|January 13, 2005
Permanent neonatal diabetes in an Asian infantJ R Porter, N J Shaw, T G Barrett, et al.
American Journal of Human Genetics|October 1, 1996
Linkage of Wolfram syndrome to chromosome 4p16.1 and evidence for heterogeneityD A Collier, T G Barrett, D Curtis, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 21, 2018
Continuing rise of Type 2 diabetes incidence in children and young people in the UKT P Candler, O Mahmoud, R M Lynn, et al.
Clinical Endocrinology|January 27, 2005
Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasiaL A Rainbow, S A Rees, M G Shaikh, et al.
Orphanet Journal of Rare Diseases|February 11, 2016
Os odontoideum in wolcott-rallison syndrome: a case series of 4 patientsR P Dias, C R Buchanan, N Thomas, et al.
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