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G N Wilson

Showing results (41-50 of 88) with videos related to

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The New England Journal of Medicine|October 25, 1984
Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomesN S Datta, G N Wilson, A K Hajra
Pathology and Immunopathology Research|January 1, 1988
Chondrodysplasia punctatas and the peroxisomopathies: overlapping syndrome communitiesG N Wilson, R D Holmes, A K Hajra
Community Dental Health|December 1, 1987
The dental needs and demands of an elderly population living in care in South CumbriaG N Wilson, D J Salway, E A McLaughlin
American Journal of Medical Genetics|July 1, 1988
Peroxisomal disorders: clinical commentary and future prospectsG N Wilson, R D Holmes, A K Hajra
American Journal of Medical Genetics|November 1, 1993
Three cases of dup(10p)/del(10q) syndrome resulting from maternal pericentric inversionA S Kulharya, N R Schneider, G N Wilson
American Journal of Medical Genetics|April 15, 1993
Index finger hyperphalangy and multiple anomalies: Catel-Manzke syndrome?G N Wilson, T E King, G S Brookshire
Clinical Genetics|March 1, 1983
Partial trisomy 2qR E Schumacher, A P Rocchini, G N Wilson
The New England Journal of Medicine|June 18, 1987
Peroxisomal enzyme deficiency in the Conradi-Hunerman form of chondrodysplasia punctataR D Holmes, G N Wilson, A K Hajra
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1975
Strand-selective transcription of globin genes in rabbit erythroid cells and chromatinG N Wilson, A W Steggles, A W Nienhuis
American Journal of Medical Genetics|September 11, 1991
Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndromeG N Wilson, R H Squires, A G Weinberg
Pageof 9

Showing results (41-50 of 88) with videos related to

Sort By:
Pageof 9
The New England Journal of Medicine|October 25, 1984
Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomesN S Datta, G N Wilson, A K Hajra
Pathology and Immunopathology Research|January 1, 1988
Chondrodysplasia punctatas and the peroxisomopathies: overlapping syndrome communitiesG N Wilson, R D Holmes, A K Hajra
Community Dental Health|December 1, 1987
The dental needs and demands of an elderly population living in care in South CumbriaG N Wilson, D J Salway, E A McLaughlin
American Journal of Medical Genetics|July 1, 1988
Peroxisomal disorders: clinical commentary and future prospectsG N Wilson, R D Holmes, A K Hajra
American Journal of Medical Genetics|November 1, 1993
Three cases of dup(10p)/del(10q) syndrome resulting from maternal pericentric inversionA S Kulharya, N R Schneider, G N Wilson
American Journal of Medical Genetics|April 15, 1993
Index finger hyperphalangy and multiple anomalies: Catel-Manzke syndrome?G N Wilson, T E King, G S Brookshire
Clinical Genetics|March 1, 1983
Partial trisomy 2qR E Schumacher, A P Rocchini, G N Wilson
The New England Journal of Medicine|June 18, 1987
Peroxisomal enzyme deficiency in the Conradi-Hunerman form of chondrodysplasia punctataR D Holmes, G N Wilson, A K Hajra
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1975
Strand-selective transcription of globin genes in rabbit erythroid cells and chromatinG N Wilson, A W Steggles, A W Nienhuis
American Journal of Medical Genetics|September 11, 1991
Keratitis, hepatitis, ichthyosis, and deafness: report and review of KID syndromeG N Wilson, R H Squires, A G Weinberg
Pageof 9