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Paediatrics & Child Health
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April 2, 2013
Wisdom: What is it?
James C Haworth
American Journal of Human Genetics
|
November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency
Andreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Paediatrics & Child Health
|
January 5, 2010
Congenital rickets caused by maternal vitamin D deficiency
A Micheil Innes, Molly M Seshia, Chitra Prasad, et al.
Molecular Genetics and Metabolism
|
February 17, 2009
The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations
Cheryl R Greenberg, Louise A Dilling, G Robert Thompson, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Paediatrics & Child Health
|
April 2, 2013
Wisdom: What is it?
James C Haworth
American Journal of Human Genetics
|
November 24, 2001
Mutations in the proenteropeptidase gene are the molecular cause of congenital enteropeptidase deficiency
Andreas Holzinger, Esther M Maier, Cornelius Bück, et al.
Paediatrics & Child Health
|
January 5, 2010
Congenital rickets caused by maternal vitamin D deficiency
A Micheil Innes, Molly M Seshia, Chitra Prasad, et al.
Molecular Genetics and Metabolism
|
February 17, 2009
The paradox of the carnitine palmitoyltransferase type Ia P479L variant in Canadian Aboriginal populations
Cheryl R Greenberg, Louise A Dilling, G Robert Thompson, et al.
Page
of 1