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Traffic (Copenhagen, Denmark)
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January 25, 2012
Role of protein kinase d in Golgi exit and lysosomal targeting of the transmembrane protein, Mcoln1
David L Marks, Eileen L Holicky, Christine L Wheatley, et al.
Immunogenetics
|
July 13, 2014
Age-dependent HLA profiles of the Israeli population: impact on hematopoietic cell donor recruitment and availability
Moshe Israeli, Machteld Oudshoorn, Geert W Haasnoot, et al.
Molecular Genetics and Metabolism
|
March 19, 2005
A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans
Ronen Spiegel, Gideon Bach, Vivi Sury, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2004
Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population
Josef Ekstein, Berish Y Rubin, Sylvia L Anderson, et al.
Molecular Genetics and Metabolism
|
April 25, 2006
When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients
Ruth Bargal, Marsha Zeigler, Bassam Abu-Libdeh, et al.
Experimental Dermatology
|
March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population
Janan Mohamad, Liat Samuelov, Natalia Malchin, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 16 results.
Traffic (Copenhagen, Denmark)
|
January 25, 2012
Role of protein kinase d in Golgi exit and lysosomal targeting of the transmembrane protein, Mcoln1
David L Marks, Eileen L Holicky, Christine L Wheatley, et al.
Immunogenetics
|
July 13, 2014
Age-dependent HLA profiles of the Israeli population: impact on hematopoietic cell donor recruitment and availability
Moshe Israeli, Machteld Oudshoorn, Geert W Haasnoot, et al.
Molecular Genetics and Metabolism
|
March 19, 2005
A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans
Ronen Spiegel, Gideon Bach, Vivi Sury, et al.
American Journal of Medical Genetics. Part A
|
August 19, 2004
Mutation frequencies for glycogen storage disease Ia in the Ashkenazi Jewish population
Josef Ekstein, Berish Y Rubin, Sylvia L Anderson, et al.
Molecular Genetics and Metabolism
|
April 25, 2006
When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients
Ruth Bargal, Marsha Zeigler, Bassam Abu-Libdeh, et al.
Experimental Dermatology
|
March 31, 2021
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population
Janan Mohamad, Liat Samuelov, Natalia Malchin, et al.
Page
of 2