Search research articles
Contact Us
Filters
Showing results (151-160 of 255) with videos related to
Page
of 26
Sort By:
American Journal of Diseases of Children (1960)
|
March 1, 1972
Fronto-metaphyseal dysplasia. A progressive disease of bone and connective tissue
D M Danks, V Mayne, R K Hall, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Succinic semialdehyde dehydrogenase deficiency--a further case
E 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 deficiency
H 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 disease
J 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 diseases
K H Choo, R G Cotton, D M Danks, et al.
Archives of Disease in Childhood
|
May 1, 1977
Prognosis of babies with neonatal hepatitis
D 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 variety
L J Sheffield, D M Danks, V Mayne, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Malonyl coenzyme A decarboxylase deficiency
G 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 spine
F 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 K12
M G Patrick, R C Cotton, D M Danks, et al.
Page
of 26
Search research articles
Search
Showing results (151-160 of 255) with videos related to
Sort By:
Page
of 26
American Journal of Diseases of Children (1960)
|
March 1, 1972
Fronto-metaphyseal dysplasia. A progressive disease of bone and connective tissue
D M Danks, V Mayne, R K Hall, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1985
Succinic semialdehyde dehydrogenase deficiency--a further case
E 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 deficiency
H 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 disease
J 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 diseases
K H Choo, R G Cotton, D M Danks, et al.
Archives of Disease in Childhood
|
May 1, 1977
Prognosis of babies with neonatal hepatitis
D 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 variety
L J Sheffield, D M Danks, V Mayne, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
Malonyl coenzyme A decarboxylase deficiency
G 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 spine
F 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 K12
M G Patrick, R C Cotton, D M Danks, et al.
Page
of 26