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Karim Ouahchi

Showing results (1-10 of 4) with videos related to

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Pharmacogenomics|December 16, 2005
Copy number variants and pharmacogenomicsKarim Ouahchi, Neal Lindeman, Charles Lee
Archives of Neurology|July 23, 2003
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaGhada El Euch-Fayache, Irfan Lalani, Rim Amouri, et al.
American Journal of Human Genetics|February 7, 2008
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degenerationMaria K Tsaousidou, Karim Ouahchi, Tom T Warner, et al.
Human Genetics|January 22, 2008
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneityAli Jalali, Kimberly A Aldinger, Ajit Chary, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Pharmacogenomics|December 16, 2005
Copy number variants and pharmacogenomicsKarim Ouahchi, Neal Lindeman, Charles Lee
Archives of Neurology|July 23, 2003
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaGhada El Euch-Fayache, Irfan Lalani, Rim Amouri, et al.
American Journal of Human Genetics|February 7, 2008
Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degenerationMaria K Tsaousidou, Karim Ouahchi, Tom T Warner, et al.
Human Genetics|January 22, 2008
Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneityAli Jalali, Kimberly A Aldinger, Ajit Chary, et al.
Pageof 1