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Author/Creator Gattas, Michael

1. The incidence, prevalence and clinical features of MECP2 duplication syndrome in Australian children. (12th February 2019)

Authors:
Giudice‐Nairn, Peter; Downs, Jenny; Wong, Kingsley; Wilson, Dylan; Ta, Daniel; Gattas, Michael; Amor, David; Thompson, Elizabeth; Kirrali‐Borri, Cathy; Ellaway, Carolyn; Leonard, Helen
Journal:
Journal of paediatrics and child health
Issue:
Volume 55:Number 11(2019)
Page Start:
1315
Record Type:
Journal Article
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2. A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations. (September 2018)

Authors:
Lee, Eric; Le, Trang; Zhu, Ying; Elakis, George; Turner, Anne; Lo, William; Venselaar, Hanka; Verrenkamp, Carol-Ann; Snow, Nicole; Mowat, David; Kirk, Edwin Philip; Sachdev, Rani; Smith, Janine; Brown, Natasha Jane; Wallis, Mathew; Barnett, Chris; McKenzie, Fiona; Freckmann, Mary-Louise; Collins,...
Journal:
Genetics in medicine
Issue:
Volume 20:Number 9(2018)
Page Start:
1061
Record Type:
Journal Article
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3. Germline ERBB3 mutation in familial non-small-cell lung carcinoma: expanding ErbB's role in oncogenesis. Issue 24 (19th July 2021)

Authors:
McInerney-Leo, Aideen M; Chew, Hui Yi; Inglis, Po-Ling; Leo, Paul J; Joseph, Shannon R; Cooper, Caroline L; Okano, Satomi; Hassall, Tim; Anderson, Lisa K; Bowman, Rayleen V; Gattas, Michael; Harris, Jessica E; Marshall, Mhairi S; Shaw, Janet G; Wheeler, Lawrie; Yang, Ian A; Brown, Matthew A; Fong...
Journal:
Human molecular genetics
Issue:
Volume 30:Issue 24(2021)
Page Start:
2393
Record Type:
Journal Article
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4. Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families. Issue 7 (6th May 2016)

Authors:
McInerney‐Leo, Aideen M.; Harris, Jessica E.; Gattas, Michael; Peach, Elizabeth E.; Sinnott, Stephen; Dudding‐Byth, Tracy; Rajagopalan, Sulekha; Barnett, Christopher P.; Anderson, Lisa K.; Wheeler, Lawrie; Brown, Matthew A.; Leo, Paul J.; Wicking, Carol; Duncan, Emma L.
Journal:
Human mutation
Issue:
Volume 37:Issue 7(2016)
Page Start:
695
Record Type:
Journal Article
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5. Cancer Risks for MLH1 and MSH2 Mutation Carriers. Issue 3 (18th February 2013)

Authors:
Dowty, James G.; Win, Aung K.; Buchanan, Daniel D.; Lindor, Noralane M.; Macrae, Finlay A.; Clendenning, Mark; Antill, Yoland C.; Thibodeau, Stephen N.; Casey, Graham; Gallinger, Steve; Marchand, Loic Le; Newcomb, Polly A.; Haile, Robert W.; Young, Graeme P.; James, Paul A.; Giles, Graham G.; Gun...
Journal:
Human mutation
Issue:
Volume 34:Issue 3(2013:Mar.)
Page Start:
490
Record Type:
Journal Article
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6. Implementing gene curation for hereditary cancer susceptibility in Australia: achieving consensus on genes with clinical utility. Issue 12 (9th November 2020)

Authors:
Tudini, Emma; Davidson, Aimee L; Dressel, Uwe; Andrews, Lesley; Antill, Yoland; Crook, Ashley; Field, Michael; Gattas, Michael; Harris, Rebecca; Kirk, Judy; Pachter, Nicholas; Salmon, Lucinda; Susman, Rachel; Townshend, Sharron; Trainer, Alison H; Tucker, Katherine M; Mitchell, Gillian; James, Pa...
Journal:
Journal of medical genetics
Issue:
Volume 58:Issue 12(2021)
Page Start:
853
Record Type:
Journal Article
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