Michael T Gabbett

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 4

Top Topics

Intellectual Disability

Top Venues

European journal of human genetics : EJHG

The New England journal of medicine

Queensland University of Technology

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Queensland University of Technology Nov 13 2017

Australia

Course Coordinator Diagnostic Genomics :: School of Biomedical Sciences

Genetic Health Queensland Jan 22 2007 - Nov 24 2017

Australia

Staff Specialist

Publications

Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Rebecca Kriukelis, Michael T Gabbett, Rachael Beswick, Aideen M McInerney-Leo, Carlie Driscoll, Karen Liddle
The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates. European journal of human genetics : EJHG (2024)
Michael T Gabbett, Johanna Laporte, Renuka Sekar, Adayapalam Nandini, Pauline McGrath, Yadav Sapkota, Peiyong Jiang, Haiqiang Zhang, Trent Burgess, Grant W Montgomery, Rossa Chiu, Nicholas M Fisk
Molecular Support for Heterogonesis Resulting in Sesquizygotic Twinning. The New England journal of medicine 380 (9) (2019)