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International Journal of Peptide and Protein Research
|
February 1, 1987
Conformational studies on polypeptide models of collagen. Poly(Gly-Pro-Val), poly(Gly-Pro-Met), poly(Gly-Val-Pro) and poly(Gly-Met-Pro)
V Guantieri, A M Tamburro, D Cabrol, et al.
International Journal of Peptide and Protein Research
|
December 1, 1984
Experimental and theoretical conformational studies on polypeptide models of collagen. Poly(Gly-Pro-Ile) and poly(Gly-Ile-Pro)
A M Tamburro, V Guantieri, D Cabrol, et al.
American Journal of Human Genetics
|
October 1, 1995
Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage
M Aminoff, E Tahvanainen, R Gräsbeck, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet
L R Gjessing, H A Lunde, T Undrum, et al.
Nature Genetics
|
March 18, 1999
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1
M Aminoff, J E Carter, R B Chadwick, et al.
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Search research articles
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Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
International Journal of Peptide and Protein Research
|
February 1, 1987
Conformational studies on polypeptide models of collagen. Poly(Gly-Pro-Val), poly(Gly-Pro-Met), poly(Gly-Val-Pro) and poly(Gly-Met-Pro)
V Guantieri, A M Tamburro, D Cabrol, et al.
International Journal of Peptide and Protein Research
|
December 1, 1984
Experimental and theoretical conformational studies on polypeptide models of collagen. Poly(Gly-Pro-Ile) and poly(Gly-Ile-Pro)
A M Tamburro, V Guantieri, D Cabrol, et al.
American Journal of Human Genetics
|
October 1, 1995
Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage
M Aminoff, E Tahvanainen, R Gräsbeck, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1986
A new patient with hyperornithinaemia, hyperammonaemia and homocitrullinuria treated early with low protein diet
L R Gjessing, H A Lunde, T Undrum, et al.
Nature Genetics
|
March 18, 1999
Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1
M Aminoff, J E Carter, R B Chadwick, et al.
Page
of 2