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Author/Creator Teo, Juliana

1. A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias. (19th July 2016)

Authors:
Roy, Noémi B. A.; Wilson, Edward A.; Henderson, Shirley; Wray, Katherine; Babbs, Christian; Okoli, Steven; Atoyebi, Wale; Mixon, Avery; Cahill, Mary R.; Carey, Peter; Cullis, Jonathan; Curtin, Julie; Dreau, Helene; Ferguson, David J. P.; Gibson, Brenda; Hall, Georgina; Mason, Joanne; Morgan, Mary...
Journal:
British journal of haematology
Issue:
Volume 175:Number 2(2016)
Page Start:
318
Record Type:
Journal Article
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2. A novel cause of DKC1‐related bone marrow failure: Partial deletion of the 3′ untranslated region. Issue 2 (26th January 2021)

Authors:
Arthur, Jonathan W.; Pickett, Hilda A.; Barbaro, Pasquale M.; Kilo, Tatjana; Vasireddy, Raja S.; Beilharz, Traude H.; Powell, David R.; Hackett, Emma L.; Bennetts, Bruce; Curtin, Julie A.; Jones, Kristi; Christodoulou, John; Reddel, Roger R.; Teo, Juliana; Bryan, Tracy M.
Journal:
EJHaem
Issue:
Volume 2:Issue 2(2021)
Page Start:
157
Record Type:
Journal Article
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3. Cardiac iron load and function in transfused patients treated with deferasirox (the MILE study). (20th September 2016)

Authors:
Ho, P. Joy; Tay, Lay; Teo, Juliana; Marlton, Paula; Grigg, Andrew; St Pierre, Tim; Brown, Greg; Badcock, Caro‐Anne; Traficante, Robert; Gervasio, Othon L.; Bowden, Donald K.
Journal:
European journal of haematology
Issue:
Volume 98:Number 2(2017:Feb.)
Page Start:
97
Record Type:
Journal Article
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4. SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature. Issue 11 (5th August 2021)

Authors:
Heeney, Matthew M.; Berhe, Simon; Campagna, Dean R.; Oved, Joseph H.; Kurre, Peter; Shaw, Peter J.; Teo, Juliana; Shanap, Mayada A.; Hassab, Hoda M.; Glader, Bertil E.; Shah, Sanjay; Yoshimi, Ayami; Ameri, Afshin; Antin, Joseph H.; Boudreaux, Jeanne; Briones, Michael; Dickerson, Kathryn E.; Ferna...
Journal:
Human mutation
Issue:
Volume 42:Issue 11(2021)
Page Start:
1367
Record Type:
Journal Article
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