Researcher
Michael T. Gabbett
Queensland University of Technology
Statistics
35 papers found
Papers authored by Michael T. Gabbett
Refreshing results…
2013
G. Elakis,
T. Roscioli,
T. C. Cox,
D. J. Moon,
H. Venselaar,
A. M. Turner,
T. Le,
E. Hackett,
A. Colley,
E. Haan,
D. Mowat,
L. Worgan,
E. P. Kirk,
R. Sachdev,
M. Gabbett 
and 24 other authors
Download from www.researchgate.net
and 24 other authors
Download from www.researchgate.net
2012
Annette F. Baas,
Michael Gabbett ,
Milan Rimac,
Minttu Kansikas,
Martine Raphael,
Rutger Aj Nievelstein,
Wayne Nicholls,
Johan Offerhaus,
Danielle Bodmer,
Annekatrin Wernstedt,
Birgit Krabichler,
Ulrich Strasser,
Minna Nyström,
Johannes Zschocke,
Stephen P. Robertson
and 2 other authors
Download from www.nature.com
,
Milan Rimac,
Minttu Kansikas,
Martine Raphael,
Rutger Aj Nievelstein,
Wayne Nicholls,
Johan Offerhaus,
Danielle Bodmer,
Annekatrin Wernstedt,
Birgit Krabichler,
Ulrich Strasser,
Minna Nyström,
Johannes Zschocke,
Stephen P. Robertson
and 2 other authors
Download from www.nature.com
2011
Maria Paola Lombardi,
Saskia Bulk,
Jacopo Celli,
Anne Lampe,
Michael T. Gabbett ,
Lillian Bomme Ousager,
Jasper J. van der Smagt,
Maria Soller,
Eva-Lena Stattin,
Marcel A. M. M. Mannens,
Robert Smigiel,
Raoul Cm Hennekam
,
Lillian Bomme Ousager,
Jasper J. van der Smagt,
Maria Soller,
Eva-Lena Stattin,
Marcel A. M. M. Mannens,
Robert Smigiel,
Raoul Cm Hennekam
Mutation update for the PORCN gene.
Download from onlinelibrary.wiley.com
Dagan Jenkins,
Gareth Baynam,
Luc De Catte,
Nursel Elcioglu,
Mt T. Gabbett ,
Louanne Hudgins,
Ja A. Hurst,
Fs S. Jehee,
Christine Oley,
Ao O. M. Wilkie
,
Louanne Hudgins,
Ja A. Hurst,
Fs S. Jehee,
Christine Oley,
Ao O. M. Wilkie
Carpenter syndrome: Extended RAB23 mutation spectrum and analysis of nonsense-mediated mRNA decay
Download from onlinelibrary.wiley.com
2010
Jennifer J. Johnston,
Julie C. Sapp,
Joyce T. Turner,
David Amor,
Salim Aftimos,
Kyrieckos A. Aleck,
Maureen Bocian,
Joann N. Bodurtha,
Gerald F. Cox,
Cynthia J. Curry,
Ruth Day,
Dian Donnai,
Michael Field,
Ikuma Fujiwara,
Michael Gabbett
and 40 other authors
and 40 other authors
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations
Download from www.ncbi.nlm.nih.gov
Adeline Jacquinet,
Marion Gerard,
Michael T. Gabbett ,
Leon Rausin,
Jean-Paul Misson,
Bjorn Menten,
Geert Mortier ,
Lionel Van Maldergem,
Alain Verloes,
François-Guillaume Debray
,
Leon Rausin,
Jean-Paul Misson,
Bjorn Menten,
Geert Mortier ,
Lionel Van Maldergem,
Alain Verloes,
François-Guillaume Debray
Temple-Baraitser syndrome: a rare and possibly unrecognized condition.
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2009
Benjamin Aaron Kamien,
Michael Terrence Gabbett
Aicardi syndrome associated with hepatoblastoma and pulmonary sequestration
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2008
Michael T. Gabbett ,
Stephen P. Robertson,
Roland Broadbent,
Salim Aftimos,
Rani Sachdev,
Marjan M. Nezarati
,
Stephen P. Robertson,
Roland Broadbent,
Salim Aftimos,
Rani Sachdev,
Marjan M. Nezarati
Characterizing the oculoauriculofrontonasal syndrome
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