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Barry Eng

Showing results (11-20 of 41) with videos related to

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Developmental Medicine and Child Neurology|April 13, 2006
Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutationsBanu Anlar, John S Waye, Barry Eng, et al.
Hemoglobin|December 24, 2005
Identification of a new delta chain hemoglobin variant in a beta-thalassemia carrier: Hb A2-mumc [delta13(a10)Ala-->Asp]Lynda Walker, Margie Patterson, Barry Eng, et al.
Hemoglobin|December 24, 2005
Characterization of a rare single alpha-globin gene deletion in a Chinese woman with Hb H diseaseBarry Eng, Robert Walsh, Lynda Walker, et al.
Hemoglobin|February 12, 2009
Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variantJohn S Waye, Lynda Walker, Lisa M Nakamura, et al.
Hemoglobin|November 9, 2016
Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin|November 29, 2017
Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin GeneJohn S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.
Hemoglobin|January 22, 2011
β+-Thalassemia trait due to a novel mutation in the β-globin gene promoter: -26 (A>C) [HBB c.-76A>C]John S Waye, Lisa M Nakamura-Garrett, Barry Eng, et al.
Hemoglobin|August 26, 2017
α<sup>0</sup>-Thalassemia Due to a 90.7 kb Deletion (- -<sup>NFLD</sup>)John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin|February 15, 2024
Splice Acceptor Mutation [<i>HBB</i>:c.93-2A > T] in a Patient with Hb S/β<sup>0</sup>-ThalassemiaJohn S Waye, Meredith Hanna, Lisa Nakamura, et al.
Hemoglobin|May 9, 2013
Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)John S Waye, Barry Eng, Laurie Hellens, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Developmental Medicine and Child Neurology|April 13, 2006
Atypical clinical course in juvenile metachromatic leukodystrophy involving novel arylsulfatase A gene mutationsBanu Anlar, John S Waye, Barry Eng, et al.
Hemoglobin|December 24, 2005
Identification of a new delta chain hemoglobin variant in a beta-thalassemia carrier: Hb A2-mumc [delta13(a10)Ala-->Asp]Lynda Walker, Margie Patterson, Barry Eng, et al.
Hemoglobin|December 24, 2005
Characterization of a rare single alpha-globin gene deletion in a Chinese woman with Hb H diseaseBarry Eng, Robert Walsh, Lynda Walker, et al.
Hemoglobin|February 12, 2009
Hb North York [beta 117(G19)His-->Asp]: a new beta chain hemoglobin variantJohn S Waye, Lynda Walker, Lisa M Nakamura, et al.
Hemoglobin|November 9, 2016
Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin|November 29, 2017
Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin GeneJohn S Waye, Meredith Hanna, Betty-Ann Hohenadel, et al.
Hemoglobin|January 22, 2011
β+-Thalassemia trait due to a novel mutation in the β-globin gene promoter: -26 (A>C) [HBB c.-76A>C]John S Waye, Lisa M Nakamura-Garrett, Barry Eng, et al.
Hemoglobin|August 26, 2017
α<sup>0</sup>-Thalassemia Due to a 90.7 kb Deletion (- -<sup>NFLD</sup>)John S Waye, Barry Eng, Meredith Hanna, et al.
Hemoglobin|February 15, 2024
Splice Acceptor Mutation [<i>HBB</i>:c.93-2A > T] in a Patient with Hb S/β<sup>0</sup>-ThalassemiaJohn S Waye, Meredith Hanna, Lisa Nakamura, et al.
Hemoglobin|May 9, 2013
Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)John S Waye, Barry Eng, Laurie Hellens, et al.
Pageof 5