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M Owada

Showing results (11-20 of 119) with videos related to

Pageof 12
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Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Disorders of phosphorylation system of lysosomal enzymes [mucolipidosis II, III]]M Owada
Ryoikibetsu Shokogun Shirizu|January 1, 1997
[Peroxisomal disorders (Zellweger syndrome)]M Owada
Ryoikibetsu Shokogun Shirizu|July 21, 2001
[Cystic fibrosis]M Owada
Ryoikibetsu Shokogun Shirizu|November 1, 2000
[Fetal iodine deficiency disorder]M Owada
Ryoikibetsu Shokogun Shirizu|January 1, 1996
[Lysosomal diseases]M Owada
Nihon Rinsho. Japanese Journal of Clinical Medicine|June 29, 1979
[Laboratory diagnosis of inborn errors of metabolism: detection of genetic carriers]M Owada
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|April 1, 1988
[Galactosemia]M Owada
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1989
[Significance of formiminoglutamic acid analysis in clinical tests]M Owada
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Maternal phenylketonuria]M Owada
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 1, 1984
[Hereditary connective tissue diseases. Mucolipidosis]M Owada
Pageof 12

Showing results (11-20 of 119) with videos related to

Sort By:
Pageof 12
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Disorders of phosphorylation system of lysosomal enzymes [mucolipidosis II, III]]M Owada
Ryoikibetsu Shokogun Shirizu|January 1, 1997
[Peroxisomal disorders (Zellweger syndrome)]M Owada
Ryoikibetsu Shokogun Shirizu|July 21, 2001
[Cystic fibrosis]M Owada
Ryoikibetsu Shokogun Shirizu|November 1, 2000
[Fetal iodine deficiency disorder]M Owada
Ryoikibetsu Shokogun Shirizu|January 1, 1996
[Lysosomal diseases]M Owada
Nihon Rinsho. Japanese Journal of Clinical Medicine|June 29, 1979
[Laboratory diagnosis of inborn errors of metabolism: detection of genetic carriers]M Owada
Tanpakushitsu Kakusan Koso. Protein, Nucleic Acid, Enzyme|April 1, 1988
[Galactosemia]M Owada
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1989
[Significance of formiminoglutamic acid analysis in clinical tests]M Owada
Ryoikibetsu Shokogun Shirizu|May 20, 1998
[Maternal phenylketonuria]M Owada
Nihon Rinsho. Japanese Journal of Clinical Medicine|May 1, 1984
[Hereditary connective tissue diseases. Mucolipidosis]M Owada
Pageof 12