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Showing results (51-60 of 54) with videos related to

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The Journal of Clinical Investigation|March 1, 1993
Lack of hormone binding in COS-7 cells expressing a mutated growth hormone receptor found in Laron dwarfismM Edery, M Rozakis-Adcock, L Goujon, et al.
Nature Genetics|May 1, 1997
A dominant-negative mutation of the growth hormone receptor causes familial short statureR M Ayling, R Ross, P Towner, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 2, 1999
New growth hormone receptor exon 9 mutation causes genetic short statureR M Ayling, R J Ross, P Towner, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptorJ Wojcik, M A Berg, N Esposito, et al.
Pageof 6

Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
The Journal of Clinical Investigation|March 1, 1993
Lack of hormone binding in COS-7 cells expressing a mutated growth hormone receptor found in Laron dwarfismM Edery, M Rozakis-Adcock, L Goujon, et al.
Nature Genetics|May 1, 1997
A dominant-negative mutation of the growth hormone receptor causes familial short statureR M Ayling, R Ross, P Towner, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|April 2, 1999
New growth hormone receptor exon 9 mutation causes genetic short statureR M Ayling, R J Ross, P Towner, et al.
The Journal of Clinical Endocrinology and Metabolism|December 16, 1998
Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptorJ Wojcik, M A Berg, N Esposito, et al.
Pageof 6