Timbs AT - Search Results

1

Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotyping.

Timbs AT, Rugless MJ, Gallienne AE, Haywood AM, Henderson SJ, Old JM. Timbs AT, et al. Hemoglobin. 2012;36(2):144-50. doi: 10.3109/03630269.2011.647998. Epub 2012 Jan 12. Hemoglobin. 2012. PMID: 22239406

2

Multiplex ligation-dependent probe amplification identification of 17 different beta-globin gene deletions (including four novel mutations) in the UK population.

Gallienne AE, Dréau HM, McCarthy J, Timbs AT, Hampson JM, Schuh A, Old JM, Henderson SJ. Gallienne AE, et al. Among authors: timbs at. Hemoglobin. 2009;33(6):406-16. doi: 10.3109/03630260903344564. Hemoglobin. 2009. PMID: 19958185

3

Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.

Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM. Henderson SJ, et al. Among authors: timbs at. Hemoglobin. 2016;40(2):75-84. doi: 10.3109/03630269.2015.1113990. Epub 2015 Dec 4. Hemoglobin. 2016. PMID: 26635043 Review.

4

A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK.

Khalil MSM, Timbs AT, Henderson SJ, Schuh A, El-Khawanky MM, Old JM. Khalil MSM, et al. Among authors: timbs at. Hemoglobin. 2020 May;44(3):195-200. doi: 10.1080/03630269.2020.1783288. Epub 2020 Jun 29. Hemoglobin. 2020. PMID: 32597250

5

Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or HBA1: c.-24C>G (or HBA2) Variants.

Khalil MSM, Timbs AT, Henderson SJ, Schuh A, Old JM. Khalil MSM, et al. Among authors: timbs at. Hemoglobin. 2020 Sep;44(5):364-367. doi: 10.1080/03630269.2020.1817755. Epub 2020 Sep 14. Hemoglobin. 2020. PMID: 32924661

6

Twelve Cases of Hb Manitoba [α102(G9)Ser→Arg]: the Fluctuation in the Variant Expression.

Khalil MSM, Timbs AT, Henderson SJ, Schuh A, Old JM. Khalil MSM, et al. Among authors: timbs at. Hemoglobin. 2020 Nov;44(6):442-445. doi: 10.1080/03630269.2020.1850473. Epub 2020 Nov 29. Hemoglobin. 2020. PMID: 33249879

7

Eight Cases of Hb Winnipeg [HBA2: c.226G>T (or HBA1)]: A Detailed Study.

Khalil MSM, Timbs AT, Henderson SJ, Schuh A, Old JM. Khalil MSM, et al. Among authors: timbs at. Hemoglobin. 2021 Jul;45(4):256-258. doi: 10.1080/03630269.2021.1976203. Epub 2021 Sep 8. Hemoglobin. 2021. PMID: 34496687

8

Eleven Cases of Hb J-Paris-I [HBA2: c.38C>A (or HBA1)]: A Stable α Chain Variant Elutes in the P3 Window on High-Performance Liquid Chromatography.

Khalil MSM, Timbs AT, Henderson SJ, Schuh A, Old JM. Khalil MSM, et al. Among authors: timbs at. Hemoglobin. 2021 Sep;45(5):322-324. doi: 10.1080/03630269.2021.2003381. Epub 2021 Nov 16. Hemoglobin. 2021. PMID: 34784833

9

Screening for clinically significant non-deletional alpha thalassaemia mutations by pyrosequencing.

Haywood A, Dreau H, Timbs A, Schuh A, Old J, Henderson S. Haywood A, et al. Ann Hematol. 2010 Dec;89(12):1215-21. doi: 10.1007/s00277-010-1013-2. Epub 2010 Jun 22. Ann Hematol. 2010. PMID: 20567827

10

A study of δ-globin gene mutations in the UK population: identification of three novel variants and development of a novel DNA test for Hb A'2.

Khalil MS, Marouf S, Element D, Timbs A, Gallienne A, Schuh A, Old JM, Henderson S. Khalil MS, et al. Hemoglobin. 2014;38(3):201-6. doi: 10.3109/03630269.2014.885908. Epub 2014 Mar 6. Hemoglobin. 2014. PMID: 24601842

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