"Moral versions" of motherhood and daughterhood in Greek-Australian family narratives

2007 ◽  
pp. 107-132 ◽  
Author(s):  
Eleni Petraki ◽  
Carolyn Baker ◽  
Michael Emmison
Keyword(s):  
Australian Family ◽  
Family Narratives

α Thalassemia british type (αα/--BRIT) in an australian family

Pathology ◽  
1986 ◽  
Vol 18 (2) ◽  
pp. 193-195 ◽  
Author(s):  
Thomas Wilkinson ◽  
J. Yakas ◽  
H. Kronenberg ◽  
R.J. Trent
Keyword(s):  
Australian Family

A second australian family with hemoglobin north shore (β134 VAL→GLU)

Pathology ◽  
1987 ◽  
Vol 19 (1) ◽  
pp. 62-63 ◽  
Author(s):  
Howard Gurney ◽  
Ibrahim Baig ◽  
Susan Gordon ◽  
Kiran Phadke ◽  
Heather Kearsley ◽  
...  
Keyword(s):  
North Shore ◽  
Australian Family

HAEMOGLOBIN J BALTIMORE INTERACTING WITH BETA‐THALASSAEMIA IN AN AUSTRALIAN FAMILY

1967 ◽  
Vol 1 (18) ◽  
pp. 907-910 ◽  
Author(s):  
T. Wilkinson ◽  
H. Kronenberg ◽  
W. A. Isaacs ◽  
H. Lehmann
Keyword(s):  
Beta Thalassaemia ◽  
Australian Family

Novel mutation in ferroportin1 is associated with autosomal dominant hemochromatosis

Blood ◽  
2002 ◽  
Vol 100 (2) ◽  
pp. 692-694 ◽  
Author(s):  
Daniel F. Wallace ◽  
Palle Pedersen ◽  
Jeannette L. Dixon ◽  
Peter Stephenson ◽  
Jeffrey W. Searle ◽  
...  
Keyword(s):  
Iron Transport ◽  
Autosomal Recessive ◽  
Iron Homeostasis ◽  
Autosomal Dominant ◽  
Novel Mutation ◽  
Hfe Gene ◽  
Excess Iron ◽  
Chromosome 1Q ◽  
Australian Family ◽  
Autosomal Recessive Pattern

Abstract Hemochromatosis is a common disorder characterized by excess iron absorption and accumulation of iron in tissues. Usually hemochromatosis is inherited in an autosomal recessive pattern and is caused by mutations in the HFE gene. Less common non-HFE–related forms of hemochromatosis have been reported and are caused by mutations in the transferrin receptor 2 gene and in a gene localized to chromosome 1q. Autosomal dominant forms of hemochromatosis have also been described. Recently, 2 mutations in theferroportin1 gene, which encodes the iron transport protein ferroportin1, have been implicated in families with autosomal dominant hemochromatosis from the Netherlands and Italy. We report the finding of a novel mutation (V162del) in ferroportin1 in an Australian family with autosomal dominant hemochromatosis. We propose that this mutation disrupts the function of the ferroportin1 protein, leading to impaired iron homeostasis and iron overload.

Report on the X-linked lymphoproliferative disease in an Australian family

1992 ◽  
Vol 28 (2) ◽  
pp. 184-189 ◽  
Author(s):  
A. M. TURNER ◽  
V. A. BERDOUKAS ◽  
V. H. TOBIAS ◽  
J. B. ZIEGLER ◽  
I. R. TOOGOOD ◽  
...  
Keyword(s):  
Lymphoproliferative Disease ◽  
Australian Family
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