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F Y Choy

Showing results (21-30 of 32) with videos related to

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American Journal of Medical Genetics|January 20, 1997
Novel insertion mutation in a non-Jewish Caucasian type 1 Gaucher disease patientF Y Choy, M L Humphries, P Ferreira
American Journal of Medical Genetics|August 1, 1987
Gaucher disease: accurate identification of asymptomatic French-Canadian carrier using nonlabeled authentic sphingolipid substrate N-palmitoyl dihydroglucocerebrosideF Y Choy, L Bouillon, C A Laurin
Journal of Medical Genetics|January 1, 1997
Gaucher disease: molecular screening of the glucocerebrosidase 1601G and 1601A alleles in Victoria, British Columbia, CanadaF Y Choy, J Linsey, P D MacLeod
American Journal of Medical Genetics|August 8, 1997
Identification of two novel and four uncommon missense mutations among chinese Gaucher disease patientsF Y Choy, M L Humphries, H Shi
Human Mutation|April 17, 1999
A novel mutation (V191G) in a German-British type 1 Gaucher disease patient. Mutations in brief no. 131. OnlineF Y Choy, M L Humphries, Y Ben-Yoseph
American Journal of Medical Genetics|December 15, 1991
Molecular analysis of Gaucher disease: screening of patients in the Montreal/Quebec regionF Y Choy, M Woo, V M Der Kaloustian
American Journal of Medical Genetics|June 24, 1998
Gaucher type 2 disease: identification of a novel transversion mutation in a French-Irish patientF Y Choy, M L Humphries, Y Ben-Yoseph
American Journal of Medical Genetics|June 15, 1991
Molecular analysis of Gaucher disease in a Vietnamese-Czechoslovak patient with high residual glucocerebrosidase activityF Y Choy, M Woo, V M Der Kaloustian
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 4, 2000
Novel point mutation (W184R) in neonatal type 2 Gaucher diseaseF Y Choy, K Wong, H D Vallance, et al.
Human Molecular Genetics|May 1, 1994
A new missense mutation in glucocerebrosidase exon 9 of a non-Jewish Caucasian type 1 Gaucher disease patientF Y Choy, C Wei, D A Applegarth, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|January 20, 1997
Novel insertion mutation in a non-Jewish Caucasian type 1 Gaucher disease patientF Y Choy, M L Humphries, P Ferreira
American Journal of Medical Genetics|August 1, 1987
Gaucher disease: accurate identification of asymptomatic French-Canadian carrier using nonlabeled authentic sphingolipid substrate N-palmitoyl dihydroglucocerebrosideF Y Choy, L Bouillon, C A Laurin
Journal of Medical Genetics|January 1, 1997
Gaucher disease: molecular screening of the glucocerebrosidase 1601G and 1601A alleles in Victoria, British Columbia, CanadaF Y Choy, J Linsey, P D MacLeod
American Journal of Medical Genetics|August 8, 1997
Identification of two novel and four uncommon missense mutations among chinese Gaucher disease patientsF Y Choy, M L Humphries, H Shi
Human Mutation|April 17, 1999
A novel mutation (V191G) in a German-British type 1 Gaucher disease patient. Mutations in brief no. 131. OnlineF Y Choy, M L Humphries, Y Ben-Yoseph
American Journal of Medical Genetics|December 15, 1991
Molecular analysis of Gaucher disease: screening of patients in the Montreal/Quebec regionF Y Choy, M Woo, V M Der Kaloustian
American Journal of Medical Genetics|June 24, 1998
Gaucher type 2 disease: identification of a novel transversion mutation in a French-Irish patientF Y Choy, M L Humphries, Y Ben-Yoseph
American Journal of Medical Genetics|June 15, 1991
Molecular analysis of Gaucher disease in a Vietnamese-Czechoslovak patient with high residual glucocerebrosidase activityF Y Choy, M Woo, V M Der Kaloustian
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 4, 2000
Novel point mutation (W184R) in neonatal type 2 Gaucher diseaseF Y Choy, K Wong, H D Vallance, et al.
Human Molecular Genetics|May 1, 1994
A new missense mutation in glucocerebrosidase exon 9 of a non-Jewish Caucasian type 1 Gaucher disease patientF Y Choy, C Wei, D A Applegarth, et al.
Pageof 4