C. Newbound

α-Thalassemia Trait Caused by Frameshift Mutations in Exon 2 of the α2-Globin Gene: HBA2:c.131delT and HBA2:c.143delA

J. Beilby, R. Ghassemifar, J. Finlayson, 2012, Hemoglobin.

Hb Lynwood [α107(G14) (–T) (α2) HBA2:c.323delT)] in Conjunction with the α3.7 Deletion Produces a Moderately Severe α-Thalassemia Phenotype

J. Beilby, R. Ghassemifar, J. Finlayson, 2011, Hemoglobin.

A molecular tool to assess the pathological relevance of alpha-globin DNA variants

J. Beilby, R. Ghassemifar, J. Finlayson, 2012, Pathology.

Experimental Characterization of Hb Flurlingen (HBA2: c.177 C > G, p.His > Gln) and Hb Boghé (HBA2: c.177 C > A, p.His > Gln) Reveals Contradictory HBA2 Expression and Translation Patterns Despite Identical Amino Acid Substitutions

R. Ghassemifar, J. Finlayson, Talal Qadah, 2015, Hemoglobin.

A Controlled Trial of Posthysterectomy Abdominal Colic

N. Johnson, M. Rashid, C. Newbound, 1993 .

Markedly discordant mitochondrial DNA and allozyme phylogenies of tube-nosed fruit bats, Nyctimene, at the Australian-Oriental biogeographical interface

R. How, S. Hisheh, L. Schmitt, 2008 .

Molecular and Cellular Characterization of a New α-Thalassemia Mutation (HBA2:c.94A>C) Generating an Alternative Splice Site and a Premature Stop Codon

J. Beilby, R. Ghassemifar, J. Finlayson, 2012, Hemoglobin.