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Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 4
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Original Article

Novel β°-Thalassemia Mutation in a Canadian Woman of British Descent (Codons 72/73, -Agtga, +T)

J. S. Waye Provincial Hemoglobinopathy DNA Diagnostic Laboratory, McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
,
B. Eng Provincial Hemoglobinopathy DNA Diagnostic Laboratory, McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
,
M. Patterson Provincial Hemoglobinopathy DNA Diagnostic Laboratory, McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
,
D. H. K. Chui Provincial Hemoglobinopathy DNA Diagnostic Laboratory, McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
&
B. J. Fernandes Mount Sinai Hospital, Toronto, Ontario, M5G 1X5, Canada
Pages 385-387 | Received 03 Jan 1997, Accepted 09 Apr 1997, Published online: 07 Jul 2009

Citations (4)

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Read on this site (1)

T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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Articles from other publishers (3)

Opeyemi S. Soremekun, Chisom Ezenwa, Itunuoluwa Isewon, Mahmoud Soliman, Omotuyi Idowu, Oyekanmi Nashiru & Segun Fatumo. (2020) Computational and drug target analysis of functional single nucleotide polymorphisms associated with Haemoglobin Subunit Beta (HBB) gene. Computers in Biology and Medicine 125, pages 104018.
Crossref
B. Eng, M. Patterson, L. Walker, D.H.K. Chui & J.S. Waye. (2001) Detection of Severe Nondeletional α -Thalassemia Mutations Using a Single-Tube Multiplex ARMS Assay . Genetic Testing 5:4, pages 327-329.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .

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