Robert W Taylor
发表
Grainne S. Gorman,
Robert W Taylor,
2014
.
Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
Katrien Stouffs,
Melanie Bahlo,
Holger Prokisch,
2016,
American journal of human genetics.
Robert W Taylor,
Robert W. Taylor,
N. Lax,
2016,
The Journal of pathology.
Leena Peltonen,
Vineta Fellman,
Anu Suomalainen,
2002,
American journal of human genetics.
Robert W Taylor,
Philip G Griffiths,
D. Turnbull,
2005,
Muscle & nerve.
Joanna Poulton,
Robert W Taylor,
Robert W. Taylor,
2013,
Human mutation.
Arnold Munnich,
Aleksandra Filipovska,
Patrick F Chinnery,
2016,
American journal of human genetics.
Thomas Meitinger,
Gabi Kastenmüller,
Jerzy Adamski,
2017,
Nature Communications.
Beril Talim,
Patrick F Chinnery,
Robert W Taylor,
2014,
JAMA.
Robert W Taylor,
Robert W. Taylor,
Michael K. Hutchinson,
2002,
European Journal of Human Genetics.
Patrick F Chinnery,
Robert W Taylor,
Robert W. Taylor,
2010,
Nature.
David C Samuels,
Patrick F Chinnery,
Robert W Taylor,
2008,
Nature Genetics.
Arnold Munnich,
Aleksandra Filipovska,
Patrick F Chinnery,
2016,
American journal of human genetics.
Robert W Taylor,
Robert W. Taylor,
J. Elson,
2010,
Wiley interdisciplinary reviews. RNA.