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D M Danks

Showing results (151-160 of 255) with videos related to

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American Journal of Diseases of Children (1960)|March 1, 1972
Fronto-metaphyseal dysplasia. A progressive disease of bone and connective tissueD M Danks, V Mayne, R K Hall, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Succinic semialdehyde dehydrogenase deficiency--a further caseE A Haan, G K Brown, D Mitchell, et al.
Journal of Medical Genetics|January 1, 1988
The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiencyH H Dahl, S Wake, R G Cotton, et al.
Archives of Disease in Childhood|May 1, 1985
Long term prognosis for babies with neonatal liver diseaseJ Deutsch, A L Smith, D M Danks, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Two-dimensional polyacrylamide gel analysis of fibroblast polypeptides: discussion of its relevance for inherited diseasesK H Choo, R G Cotton, D M Danks, et al.
Archives of Disease in Childhood|May 1, 1977
Prognosis of babies with neonatal hepatitisD M Danks, P E Campbell, A L Smith, et al.
The Journal of Pediatrics|December 1, 1976
Chondrodysplasia punctata-23 cases of a mild and relatively common varietyL J Sheffield, D M Danks, V Mayne, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Malonyl coenzyme A decarboxylase deficiencyG K Brown, R D Scholem, A Bankier, et al.
Journal of Medical Genetics|April 1, 1979
Achondroplasia and hypochondroplasia. Comments on frequency, mutation rate, and radiological features in skull and spineF Oberklaid, D M Danks, F Jensen, et al.
Biochemical Medicine|March 1, 1975
A screening test for sulphur-containing metabolites in urine using auxotrophic mutants of Escherichia coli K12M G Patrick, R C Cotton, D M Danks, et al.
Pageof 26

Showing results (151-160 of 255) with videos related to

Sort By:
Pageof 26
American Journal of Diseases of Children (1960)|March 1, 1972
Fronto-metaphyseal dysplasia. A progressive disease of bone and connective tissueD M Danks, V Mayne, R K Hall, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
Succinic semialdehyde dehydrogenase deficiency--a further caseE A Haan, G K Brown, D Mitchell, et al.
Journal of Medical Genetics|January 1, 1988
The use of restriction fragment length polymorphisms in prenatal diagnosis of dihydropteridine reductase deficiencyH H Dahl, S Wake, R G Cotton, et al.
Archives of Disease in Childhood|May 1, 1985
Long term prognosis for babies with neonatal liver diseaseJ Deutsch, A L Smith, D M Danks, et al.
Journal of Inherited Metabolic Disease|January 1, 1981
Two-dimensional polyacrylamide gel analysis of fibroblast polypeptides: discussion of its relevance for inherited diseasesK H Choo, R G Cotton, D M Danks, et al.
Archives of Disease in Childhood|May 1, 1977
Prognosis of babies with neonatal hepatitisD M Danks, P E Campbell, A L Smith, et al.
The Journal of Pediatrics|December 1, 1976
Chondrodysplasia punctata-23 cases of a mild and relatively common varietyL J Sheffield, D M Danks, V Mayne, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Malonyl coenzyme A decarboxylase deficiencyG K Brown, R D Scholem, A Bankier, et al.
Journal of Medical Genetics|April 1, 1979
Achondroplasia and hypochondroplasia. Comments on frequency, mutation rate, and radiological features in skull and spineF Oberklaid, D M Danks, F Jensen, et al.
Biochemical Medicine|March 1, 1975
A screening test for sulphur-containing metabolites in urine using auxotrophic mutants of Escherichia coli K12M G Patrick, R C Cotton, D M Danks, et al.
Pageof 26