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Showing results (71-80 of 75) with videos related to

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International Journal of Cancer|September 9, 1992
The human squamous cervical carcinoma cell line, HOG-1, is responsive to steroid hormonesJ O White, R N Jones, J D Croxtall, et al.
Human Molecular Genetics|March 18, 2005
Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5'-phosphate oxidasePhilippa B Mills, Robert A H Surtees, Michael P Champion, et al.
Human Mutation|December 26, 2003
Twenty-two novel mutations in the lysosomal alpha-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type IIMonique M P Hermans, Dik van Leenen, Marian A Kroos, et al.
Journal of Inherited Metabolic Disease|March 3, 2017
Expanding the phenotype in argininosuccinic aciduria: need for new therapiesJulien Baruteau, Elisabeth Jameson, Andrew A Morris, et al.
American Journal of Human Genetics|October 13, 2006
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome)Martin Hrebícek, Lenka Mrázová, Volkan Seyrantepe, et al.
Pageof 8

Showing results (71-80 of 75) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 75 results.
International Journal of Cancer|September 9, 1992
The human squamous cervical carcinoma cell line, HOG-1, is responsive to steroid hormonesJ O White, R N Jones, J D Croxtall, et al.
Human Molecular Genetics|March 18, 2005
Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5'-phosphate oxidasePhilippa B Mills, Robert A H Surtees, Michael P Champion, et al.
Human Mutation|December 26, 2003
Twenty-two novel mutations in the lysosomal alpha-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type IIMonique M P Hermans, Dik van Leenen, Marian A Kroos, et al.
Journal of Inherited Metabolic Disease|March 3, 2017
Expanding the phenotype in argininosuccinic aciduria: need for new therapiesJulien Baruteau, Elisabeth Jameson, Andrew A Morris, et al.
American Journal of Human Genetics|October 13, 2006
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome)Martin Hrebícek, Lenka Mrázová, Volkan Seyrantepe, et al.
Pageof 8