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Kim Debacker

Showing results (1-10 of 5) with videos related to

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Human Molecular Genetics|June 15, 2007
Fragile sites and human diseaseKim Debacker, R Frank Kooy
Plos Biology|February 25, 2012
Histone deacetylase complexes promote trinucleotide repeat expansionsKim Debacker, Aisling Frizzell, Olive Gleeson, et al.
American Journal of Human Genetics|January 20, 2007
CGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1Birgitta Winnepenninckx, Kim Debacker, Jacqueline Ramsay, et al.
Journal of Medical Genetics|May 4, 2007
FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakageKim Debacker, Birgitta Winnepenninckx, Neta Ben-Porat, et al.
Human Mutation|September 9, 2014
A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two familiesSofie Metsu, Jacqueline K Rainger, Kim Debacker, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Human Molecular Genetics|June 15, 2007
Fragile sites and human diseaseKim Debacker, R Frank Kooy
Plos Biology|February 25, 2012
Histone deacetylase complexes promote trinucleotide repeat expansionsKim Debacker, Aisling Frizzell, Olive Gleeson, et al.
American Journal of Human Genetics|January 20, 2007
CGG-repeat expansion in the DIP2B gene is associated with the fragile site FRA12A on chromosome 12q13.1Birgitta Winnepenninckx, Kim Debacker, Jacqueline Ramsay, et al.
Journal of Medical Genetics|May 4, 2007
FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakageKim Debacker, Birgitta Winnepenninckx, Neta Ben-Porat, et al.
Human Mutation|September 9, 2014
A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two familiesSofie Metsu, Jacqueline K Rainger, Kim Debacker, et al.
Pageof 1