Search research articles
Contact Us
Filters
Showing results (1-10 of 34) with videos related to
Page
of 4
Sort By:
Current Opinion in Neurology
|
November 28, 2001
Neurodegenerative disease: the neuronal ceroid lipofuscinoses (Batten disease)
H M Mitchison, S E Mole
Paediatric Respiratory Reviews
|
June 30, 2004
Cilia, primary ciliary dyskinesia and molecular genetics
R Chodhari, H M Mitchison, M Meeks
Human Mutation
|
September 8, 1999
Molecular basis of the neuronal ceroid lipofuscinoses: mutations in CLN1, CLN2, CLN3, and CLN5
S E Mole, H M Mitchison, P B Munroe
Proceedings. Biological Sciences
|
December 24, 2004
Handedness and situs inversus in primary ciliary dyskinesia
I C McManus, N Martin, G F Stubbings, et al.
American Journal of Medical Genetics
|
June 5, 1995
Analysis of Batten disease candidate genes STP and STM
P B Munroe, H M Mitchison, T P Dooley, et al.
Journal of Medical Genetics
|
December 1, 1996
Rapid diagnostic test for the major mutation underlying Batten disease
I Järvelä, H M Mitchison, P B Munroe, et al.
The Journal of General Virology
|
August 1, 1990
The expression of the adenovirus 12 early region 1B 19K protein using a recombinant simian virus 40 system
H M Mitchison, R J Grand, P J Byrd, et al.
FEBS Letters
|
December 9, 1996
A model for Batten disease protein CLN3: functional implications from homology and mutations
R W Janes, P B Munroe, H M Mitchison, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 9, 2001
High resolution MRI reveals global changes in brains of Cln3 mutant mice
N D Greene, M F Lythgoe, D L Thomas, et al.
Lancet (London, England)
|
April 13, 1996
Prenatal diagnosis of Batten's disease
P B Munroe, J Rapola, H M Mitchison, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
Current Opinion in Neurology
|
November 28, 2001
Neurodegenerative disease: the neuronal ceroid lipofuscinoses (Batten disease)
H M Mitchison, S E Mole
Paediatric Respiratory Reviews
|
June 30, 2004
Cilia, primary ciliary dyskinesia and molecular genetics
R Chodhari, H M Mitchison, M Meeks
Human Mutation
|
September 8, 1999
Molecular basis of the neuronal ceroid lipofuscinoses: mutations in CLN1, CLN2, CLN3, and CLN5
S E Mole, H M Mitchison, P B Munroe
Proceedings. Biological Sciences
|
December 24, 2004
Handedness and situs inversus in primary ciliary dyskinesia
I C McManus, N Martin, G F Stubbings, et al.
American Journal of Medical Genetics
|
June 5, 1995
Analysis of Batten disease candidate genes STP and STM
P B Munroe, H M Mitchison, T P Dooley, et al.
Journal of Medical Genetics
|
December 1, 1996
Rapid diagnostic test for the major mutation underlying Batten disease
I Järvelä, H M Mitchison, P B Munroe, et al.
The Journal of General Virology
|
August 1, 1990
The expression of the adenovirus 12 early region 1B 19K protein using a recombinant simian virus 40 system
H M Mitchison, R J Grand, P J Byrd, et al.
FEBS Letters
|
December 9, 1996
A model for Batten disease protein CLN3: functional implications from homology and mutations
R W Janes, P B Munroe, H M Mitchison, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 9, 2001
High resolution MRI reveals global changes in brains of Cln3 mutant mice
N D Greene, M F Lythgoe, D L Thomas, et al.
Lancet (London, England)
|
April 13, 1996
Prenatal diagnosis of Batten's disease
P B Munroe, J Rapola, H M Mitchison, et al.
Page
of 4