Publications by authors named "Betty-Ann Hohenadel"

10Publications

Characterization of Two Novel Deletions Involving the 5' Region of the β-Globin Gene.

Hemoglobin 2017 Jul - Nov;41(4-6):239-242. Epub 2017 Nov 28.

a Hamilton Regional Laboratory Medicine Program , Hamilton Health Sciences , Hamilton , ON , Canada.

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August 2018

α-Thalassemia Due to a 90.7 kb Deletion (- -).

Hemoglobin 2017 May 13;41(3):218-219. Epub 2017 Sep 13.

a Hamilton Regional Laboratory Medicine Program , Hamilton Health Sciences , Hamilton , Ontario , Canada.

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May 2017

Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A).

Hemoglobin 2016 Sep;40(5):369-370

a Hamilton Regional Laboratory Medicine Program , Hamilton Health Sciences , Hamilton , Ontario , Canada.

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September 2016

Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion.

Hemoglobin 2015 8;39(5):368-70. Epub 2015 Jul 8.

a Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences , Hamilton , Ontario , Canada.

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June 2016

α(+)-Thalassemia Due to a Frameshift Mutation of the α2-Globin Gene [codons 55/56 (+T) or HBA2: c.168dup].

Hemoglobin 2015 21;39(3):209-10. Epub 2015 Apr 21.

Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences , Hamilton, Ontario , Canada .

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March 2016

Hb S/β+-thalassemia due to Hb sickle and a novel deletion of DNase I hypersensitive sites HS3 and HS4 of the β locus control region.

Haematologica 2015 May 14;100(5):e166-8. Epub 2015 Feb 14.

Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada Department of Pathology and Molecular Medicine, McMaster University, Hamilton, Ontario, Canada

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May 2015

Non-thalassemic phenotype associated with the -83 (G > A) mutation of the β-globin gene promoter (HBB: c.-133G > A).

Hemoglobin 2014 ;38(6):447-8

Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences , Hamilton, Ontario , Canada .

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July 2015

Mild β(+)-thalassemia associated with two linked sequence variants: IVS-II-839 (T>C) and IVS-II-844 (C>A).

Hemoglobin 2013 8;37(4):378-86. Epub 2013 May 8.

Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada.

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January 2014

Normal Hb A2 β-thalassemia trait: frameshift mutation (HBB: c.187_251dup) in cis with the Hb A2' δ-globin gene missense mutation (HBD: c.49G>C).

Hemoglobin 2013 11;37(2):201-4. Epub 2013 Feb 11.

Hamilton Regional Laboratory Medicine Program, Hamilton Health Sciences, Hamilton, Ontario, Canada.

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September 2013