Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Barry Eng

Showing results (1-10 of 41) with videos related to

Pageof 5
Sort By:
Hemoglobin|May 14, 2008
Frameshift mutation in the alpha2-globin gene causing alpha+ -thalassemia: codon 49 (-GC)Barry Eng, John S Waye
Hemoglobin|March 2, 2012
α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT]John S Waye, Lynda Walker, Barry Eng
Hemoglobin|February 12, 2009
Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG)Barry Eng, Lynda Walker, John S Waye
Hemoglobin|December 5, 2009
Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian familiesIndu Voruganti, Barry Eng, John S Waye
Human Biology|October 7, 2003
Hypersensitive PCR, ancient human mtDNA, and contaminationDongya Y Yang, Barry Eng, Shelley R Saunders
The Journal of Applied Laboratory Medicine|February 25, 2021
Multiplex Allele-Specific PCR for Simultaneous Detection of H63D and C282Y HFE Mutations in Hereditary HemochromatosisHeleen H Arts, Barry Eng, John S Waye
Prenatal Diagnosis|April 19, 2007
Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS) by DHCR7 mutation analysisJohn S Waye, Barry Eng, Małgorzata J M Nowaczyk
Hemoglobin|December 24, 2005
High Hb A2 beta-thalassemia due to a 468 bp deletion in a patient with Hb S/beta-thalassemiaMargie Patterson, Lynda Walker, Barry Eng, et al.
Hemoglobin|December 5, 2009
alpha-Thalassemia caused by two novel splice mutations of the alpha2-globin gene: IVS-I-1 (G>A and G>T)John S Waye, Barry Eng, Fabrizio Dutly, et al.
Hemoglobin|March 17, 2007
High oxygen affinity hemoglobin variant in a Canadian family: Hb Bunbury [beta94(FG1)Asp-->Asn, GAC-->AAC]Lynda Walker, Barry Eng, Andrew McFarlane, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Hemoglobin|May 14, 2008
Frameshift mutation in the alpha2-globin gene causing alpha+ -thalassemia: codon 49 (-GC)Barry Eng, John S Waye
Hemoglobin|March 2, 2012
α(+)-Thalassemia trait caused by a frameshift mutation in exon 2 of the α2-globin gene [HBA2 c.244delT]John S Waye, Lynda Walker, Barry Eng
Hemoglobin|February 12, 2009
Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG)Barry Eng, Lynda Walker, John S Waye
Hemoglobin|December 5, 2009
Molecular characterization of a novel 55.1 kb (G)gamma((A)gammadeltabeta)(0)-thalassemia deletion in two Canadian familiesIndu Voruganti, Barry Eng, John S Waye
Human Biology|October 7, 2003
Hypersensitive PCR, ancient human mtDNA, and contaminationDongya Y Yang, Barry Eng, Shelley R Saunders
The Journal of Applied Laboratory Medicine|February 25, 2021
Multiplex Allele-Specific PCR for Simultaneous Detection of H63D and C282Y HFE Mutations in Hereditary HemochromatosisHeleen H Arts, Barry Eng, John S Waye
Prenatal Diagnosis|April 19, 2007
Prenatal diagnosis of Smith-Lemli-Opitz syndrome (SLOS) by DHCR7 mutation analysisJohn S Waye, Barry Eng, Małgorzata J M Nowaczyk
Hemoglobin|December 24, 2005
High Hb A2 beta-thalassemia due to a 468 bp deletion in a patient with Hb S/beta-thalassemiaMargie Patterson, Lynda Walker, Barry Eng, et al.
Hemoglobin|December 5, 2009
alpha-Thalassemia caused by two novel splice mutations of the alpha2-globin gene: IVS-I-1 (G>A and G>T)John S Waye, Barry Eng, Fabrizio Dutly, et al.
Hemoglobin|March 17, 2007
High oxygen affinity hemoglobin variant in a Canadian family: Hb Bunbury [beta94(FG1)Asp-->Asn, GAC-->AAC]Lynda Walker, Barry Eng, Andrew McFarlane, et al.
Pageof 5