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American Journal of Human Genetics
|
May 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood
J L Van Hove, W Zhang, S G Kahler, et al.
Pediatrics
|
April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients
K M Gibson, E Christensen, C Jakobs, et al.
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of 2
Search research articles
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Showing results (11-20 of 12) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 12 results.
American Journal of Human Genetics
|
May 1, 1993
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood
J L Van Hove, W Zhang, S G Kahler, et al.
Pediatrics
|
April 1, 1997
The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-hydroxybutyric aciduria): case reports of 23 new patients
K M Gibson, E Christensen, C Jakobs, et al.
Page
of 2