M. Mohamed
发表
Mustaq Ahmed,
F Lucy Raymond,
Martin McKibbin,
2006,
American journal of human genetics.
Colin A. Johnson,
G. Mardon,
G. Fishman,
2012,
Nature Genetics.
K. Springell,
M. Mohamed,
M. McKibbin,
2010,
Archives of ophthalmology.
M. Mohamed,
L. Pelosini,
S. Rajak,
2009,
Archives of ophthalmology.
M. Mohamed,
S. Anand,
O. Backhouse,
2006,
Ophthalmology.
M. Salto‐Tellez,
T. Aung,
M. Srinivasan,
2006,
Nature Genetics.
M. Mohamed,
J. Marshall,
L. Pelosini,
2013,
Retina.
S. S. Mann,
M. Mohamed,
D. Laidlaw,
2015,
British Journal of Ophthalmology.
M. Mohamed,
M. McKibbin,
C. Inglehearn,
2022,
Molecular vision.
Macular spectral domain optical coherence tomography findings in Tanzanian endemic optic neuropathy.
G. Plant,
O. Mahroo,
M. Mohamed,
2013,
Brain : a journal of neurology.
G. Plant,
O. Mahroo,
M. Mohamed,
2014,
Ophthalmology.
M. Mohamed,
B. Gupta,
Moin D. Mohamed,
2011,
Ophthalmologica.
T. Williamson,
O. Mahroo,
M. Mohamed,
2016,
European journal of ophthalmology.
T. Williamson,
O. Mahroo,
M. Mohamed,
2015,
Retina.
M. Mohamed,
Jonathan Virgo,
2020,
Eye.
M. Mohamed,
M. Stanford,
E. Graham,
2010,
Archives of ophthalmology.
O. Mahroo,
M. Mohamed,
R. McDonald,
2014,
Ocular immunology and inflammation.
Colin A. Johnson,
A. Markham,
M. Mohamed,
2011,
Investigative ophthalmology & visual science.
Colin A. Johnson,
G. Taylor,
M. Mohamed,
2011,
Human molecular genetics.
M. Mohamed,
T. Kwong,
2014,
British journal of clinical pharmacology.
John Bradbury,
Eamonn Sheridan,
Rohit Shetty,
2013,
American journal of human genetics.
D. Burt,
Jacqueline Smith,
D. Morrice,
2003,
Molecular vision.
M. Gentle,
D. Burt,
Jacqueline Smith,
2003,
Molecular vision.
M. Gentle,
D. Burt,
Jacqueline Smith,
2003
.
John Bradbury,
Eamonn Sheridan,
Carmel Toomes,
2013,
Molecular vision.
A. Bird,
O. Mahroo,
Nikolas Pontikos,
2020,
Progress in Retinal and Eye Research.
M. Mohamed,
C. Inglehearn,
E. Sheridan,
2004,
Journal of Medical Genetics.
M. Mohamed,
M. McKibbin,
C. Inglehearn,
2003,
The British journal of ophthalmology.
O. Mahroo,
M. Mohamed,
E. Gavin,
2012,
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.
T. Strom,
J. Veltman,
R. Roepman,
2007,
Nature Genetics.
C. Hammond,
K. Williams,
O. Mahroo,
2017,
Graefe's Archive for Clinical and Experimental Ophthalmology.
Alan Bird,
Michel Michaelides,
Anthony T. Moore,
2016,
Progress in Retinal and Eye Research.
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma.
Colin A. Johnson,
G. Taylor,
J. Craig,
2011,
American journal of human genetics.
M. Mohamed,
M. McKibbin,
C. Inglehearn,
2003,
European Journal of Human Genetics.
O. Mahroo,
P. Hysi,
M. Mohamed,
2017,
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.
S. Harding,
S. Sivaprasad,
T. Peto,
2020,
The Lancet.
M. Mohamed,
M. McKibbin,
C. Inglehearn,
2008,
Molecular vision.
M. Mohamed,
Vijaya Jojo,
2012,
Retina.
D. Mackey,
K. Hayashi,
A. Markham,
2010,
American journal of human genetics.
M. Mohamed,
S. Parvizi,
B. Gupta,
2011,
International Ophthalmology.
S. Sivaprasad,
M. Gulliford,
M. Mohamed,
2012,
PloS one.
M. Mohamed,
Anish Dhital,
2012,
Eye.
Xinjing Wang,
F. Raymond,
G. Arno,
2018,
Investigative ophthalmology & visual science.
D. Morrice,
M. Mohamed,
I. Paton,
2022
.
S. Sivaprasad,
M. Gulliford,
M. Mohamed,
2009,
Diabetic medicine : a journal of the British Diabetic Association.