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D O Robinson

Showing results (31-40 of 49) with videos related to

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Human Genetics|May 1, 1994
Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophyD J Bunyan, D O Robinson, A L Collins, et al.
Diabetes|August 3, 2000
Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetesI K Temple, R J Gardner, D J Mackay, et al.
Journal of Medical Genetics|May 5, 1999
A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndromeD O Robinson, P Dalton, P A Jacobs, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathyS R Hammans, D O Robinson, C Moutou, et al.
The Journal of Biological Chemistry|April 12, 2001
Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitusA Varrault, B Bilanges, D J Mackay, et al.
Journal of Medical Genetics|April 16, 1999
Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6qR J Gardner, A J Mungall, I Dunham, et al.
Brain : a Journal of Neurology|February 27, 2001
Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK populationM E Hill, G A Creed, T F McMullan, et al.
Annals of Human Genetics|July 1, 1990
A cytogenetic and molecular reappraisal of a series of patients with Turner's syndromeP A Jacobs, P R Betts, A E Cockwell, et al.
Human Genetics|April 6, 2002
Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitusD J G Mackay, A-M Coupe, J P H Shield, et al.
Clinical Genetics|September 8, 2011
Systematic screening of FBN1 gene unclassified missense variants for splice abnormalitiesD O Robinson, F Lin, M Lyon, et al.
Pageof 5

Showing results (31-40 of 49) with videos related to

Sort By:
Pageof 5
Human Genetics|May 1, 1994
Germline and somatic mosaicism in a female carrier of Duchenne muscular dystrophyD J Bunyan, D O Robinson, A L Collins, et al.
Diabetes|August 3, 2000
Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetesI K Temple, R J Gardner, D J Mackay, et al.
Journal of Medical Genetics|May 5, 1999
A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndromeD O Robinson, P Dalton, P A Jacobs, et al.
Neuromuscular Disorders : NMD|March 14, 2000
A clinical and genetic study of a manifesting heterozygote with X-linked myotubular myopathyS R Hammans, D O Robinson, C Moutou, et al.
The Journal of Biological Chemistry|April 12, 2001
Characterization of the methylation-sensitive promoter of the imprinted ZAC gene supports its role in transient neonatal diabetes mellitusA Varrault, B Bilanges, D J Mackay, et al.
Journal of Medical Genetics|April 16, 1999
Localisation of a gene for transient neonatal diabetes mellitus to an 18.72 cR3000 (approximately 5.4 Mb) interval on chromosome 6qR J Gardner, A J Mungall, I Dunham, et al.
Brain : a Journal of Neurology|February 27, 2001
Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK populationM E Hill, G A Creed, T F McMullan, et al.
Annals of Human Genetics|July 1, 1990
A cytogenetic and molecular reappraisal of a series of patients with Turner's syndromeP A Jacobs, P R Betts, A E Cockwell, et al.
Human Genetics|April 6, 2002
Relaxation of imprinted expression of ZAC and HYMAI in a patient with transient neonatal diabetes mellitusD J G Mackay, A-M Coupe, J P H Shield, et al.
Clinical Genetics|September 8, 2011
Systematic screening of FBN1 gene unclassified missense variants for splice abnormalitiesD O Robinson, F Lin, M Lyon, et al.
Pageof 5