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D. A. Dyment
D. A. Dyment
Curtin University
Biology
Genetics
Chromosomal inversion
Frameshift mutation
Scoliosis
2
Papers
13
Citations
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Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndrome
2017
European Journal of Medical Genetics
P. Y B Au
L. Huang
Stephanie Broley
L. Gallagher
E. Creede
D. Lahey
S. Ordorica
K. Mina
Kym M. Boycott
Gareth Baynam
D. A. Dyment
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Citations (7)
Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1
2017
Journal of Human Genetics
Priya T Bhola
Taila Hartley
Eric Bareke
K. Boycott
Alex MacKenzie
Jacek Majewski
Michael Brudno
Dennis E. Bulman
D. A. Dyment
Kym M. Boycott
Sarah M. Nikkel
David A. Dyment
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Citations (6)
1