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R G F Gray

Showing results (1-10 of 5) with videos related to

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Journal of Medical Genetics|March 19, 2002
The frequency of mtDNA 8994 polymorphism and detection of the NARP 8993 mutationR G F Gray, P A Davies, A Marshall, et al.
The British Journal of Dermatology|August 14, 2002
Mild ichthyosis in a 4-year-old boy with multiple sulphatase deficiencyA Loffeld, R G F Gray, S H Green, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Mutation screening for tyrosinaemia type IS K Heath, R G F Gray, P McKiernan, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Prenatal diagnosis of succinate semialdehyde dehydrogenase deficiency in non-identical twinsI A Aligianis, P A Farndon, R G F Gray, et al.
Developmental Medicine and Child Neurology|January 19, 2008
Practical difficulties in the diagnosis of transient non-ketotic hyperglycinaemiaT F Lang, J R Parr, E E Matthews, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Journal of Medical Genetics|March 19, 2002
The frequency of mtDNA 8994 polymorphism and detection of the NARP 8993 mutationR G F Gray, P A Davies, A Marshall, et al.
The British Journal of Dermatology|August 14, 2002
Mild ichthyosis in a 4-year-old boy with multiple sulphatase deficiencyA Loffeld, R G F Gray, S H Green, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Mutation screening for tyrosinaemia type IS K Heath, R G F Gray, P McKiernan, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
Prenatal diagnosis of succinate semialdehyde dehydrogenase deficiency in non-identical twinsI A Aligianis, P A Farndon, R G F Gray, et al.
Developmental Medicine and Child Neurology|January 19, 2008
Practical difficulties in the diagnosis of transient non-ketotic hyperglycinaemiaT F Lang, J R Parr, E E Matthews, et al.
Pageof 1