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Dorothy Trump

Showing results (21-30 of 27) with videos related to

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Human Mutation|May 3, 2006
Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxaAndrew J Lotery, Dominique Baas, Caroline Ridley, et al.
Investigative Ophthalmology & Visual Science|December 17, 2009
Structural effects of fibulin 5 missense mutations associated with age-related macular degeneration and cutis laxaRichard P O Jones, Caroline Ridley, Thomas A Jowitt, et al.
The Journal of Biological Chemistry|July 21, 2009
Fibulin 5 forms a compact dimer in physiological solutionsRichard P O Jones, Ming-Chuan Wang, Thomas A Jowitt, et al.
Human Mutation|January 29, 2003
Mutations in the CACNA1F and NYX genes in British CSNBX familiesIlaria Zito, Louise E Allen, Reshma J Patel, et al.
European Journal of Human Genetics : EJHG|August 13, 2002
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genesAnnick Toutain, Benoît Dessay, Nathalie Ronce, et al.
American Journal of Human Genetics|May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndromeLionel Willatt, James Cox, John Barber, et al.
American Journal of Human Genetics|April 2, 2013
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered proteaseEmma M Jenkinson, Atteeq U Rehman, Tom Walsh, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Human Mutation|May 3, 2006
Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxaAndrew J Lotery, Dominique Baas, Caroline Ridley, et al.
Investigative Ophthalmology & Visual Science|December 17, 2009
Structural effects of fibulin 5 missense mutations associated with age-related macular degeneration and cutis laxaRichard P O Jones, Caroline Ridley, Thomas A Jowitt, et al.
The Journal of Biological Chemistry|July 21, 2009
Fibulin 5 forms a compact dimer in physiological solutionsRichard P O Jones, Ming-Chuan Wang, Thomas A Jowitt, et al.
Human Mutation|January 29, 2003
Mutations in the CACNA1F and NYX genes in British CSNBX familiesIlaria Zito, Louise E Allen, Reshma J Patel, et al.
European Journal of Human Genetics : EJHG|August 13, 2002
Refinement of the NHS locus on chromosome Xp22.13 and analysis of five candidate genesAnnick Toutain, Benoît Dessay, Nathalie Ronce, et al.
American Journal of Human Genetics|May 27, 2005
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndromeLionel Willatt, James Cox, John Barber, et al.
American Journal of Human Genetics|April 2, 2013
Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered proteaseEmma M Jenkinson, Atteeq U Rehman, Tom Walsh, et al.
Pageof 3