Hohenadel BA - Search Results

1

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

Waye JS, Eng B, Got T, Hanna M, Hohenadel BA, Nakamura LM, Walker L. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2015;39(5):368-70. doi: 10.3109/03630269.2015.1057736. Epub 2015 Jul 8. Hemoglobin. 2015. PMID: 26154945

2

Characterization of three novel delta chain hemoglobin variants and two delta-thalassemia alleles.

Frischknecht H, Troxler H, Dutly F, Walker L, Hohenadel BA, Eng B, Waye JS. Frischknecht H, et al. Among authors: hohenadel ba. Hemoglobin. 2010;34(4):374-82. doi: 10.3109/03630269.2010.500966. Hemoglobin. 2010. PMID: 20642335

3

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).

Waye JS, Eng B, Hellens L, Hohenadel BA, Nakamura LM, Walker L. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2013;37(2):201-4. doi: 10.3109/03630269.2012.763171. Epub 2013 Feb 11. Hemoglobin. 2013. PMID: 23398055

4

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

Waye JS, Eng B, Hellens L, Hohenadel BA, Nakamura LM, Walker L. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2013;37(4):378-86. doi: 10.3109/03630269.2013.788511. Epub 2013 May 8. Hemoglobin. 2013. PMID: 23651435

5

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

Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura LN, Walker L. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2014;38(6):447-8. doi: 10.3109/03630269.2014.976417. Hemoglobin. 2014. PMID: 25405919

6

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.

Amid A, Cheong M, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L, Odame I, Kirby-Allen M, Waye JS. Amid A, et al. Among authors: hohenadel ba. Haematologica. 2015 May;100(5):e166-8. doi: 10.3324/haematol.2014.117408. Epub 2015 Feb 14. Haematologica. 2015. PMID: 25682598 Free PMC article. No abstract available.

7

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

Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura LM, Walker L. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2015;39(3):209-10. doi: 10.3109/03630269.2015.1030410. Epub 2015 Apr 21. Hemoglobin. 2015. PMID: 25897479

8

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

Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura L, Walker L. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2016 Sep;40(5):369-370. doi: 10.1080/03630269.2016.1236028. Hemoglobin. 2016. PMID: 27821014

9

α⁰-Thalassemia Due to a 90.7 kb Deletion (- -^NFLD).

Waye JS, Eng B, Hanna M, Hohenadel BA, Nakamura L, Walker L. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2017 May;41(3):218-219. doi: 10.1080/03630269.2017.1369987. Epub 2017 Sep 13. Hemoglobin. 2017. PMID: 28838269

10

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

Waye JS, Hanna M, Hohenadel BA, Nakamura L, Walker L, Eng B. Waye JS, et al. Among authors: hohenadel ba. Hemoglobin. 2017 Jul-Nov;41(4-6):239-242. doi: 10.1080/03630269.2017.1397015. Epub 2017 Nov 28. Hemoglobin. 2017. PMID: 29182041

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