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Journal of the Royal Army Medical Corps
|
February 19, 2014
Dieulafoy lesion presenting as severe anaemia in a soldier
Robert M W Burley, I Gavrielides
Annals of Human Genetics
|
November 6, 1998
A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients
J M Young, M W Burley, S J Jeremiah, et al.
Annals of Human Genetics
|
May 1, 1982
Mapping studies on human mitochondrial glutamate oxaloacetate transaminase
S J Jeremiah, S Povey, M W Burley, et al.
Annals of Human Genetics
|
February 12, 1998
Mapping ESTs to the TSC1 candidate interval by use of the 'Science 96' transcript map
J Wolfe, S Jeremiah, J Young, et al.
Human Immunology
|
June 1, 1989
HLA class III haplotypes in multicase rheumatoid arthritis families
A H Fielder, W Ollier, D K Lord, et al.
Lancet (London, England)
|
July 25, 2000
Non-penetrance in tuberous sclerosis
J P Osborne, A C Jones, M W Burley, et al.
Neurology
|
October 27, 2004
The -1021C->T DBH gene variant is not associated with epilepsy or antiepileptic drug response
C Depondt, H R Cock, D G Healy, et al.
Human Immunology
|
May 1, 1988
C4 complement allotypes in juvenile dermatomyositis
S A Robb, A H Fielder, C E Saunders, et al.
Annals of Human Genetics
|
May 1, 1994
Two loci for tuberous sclerosis: one on 9q34 and one on 16p13
S Povey, M W Burley, J Attwood, et al.
Human Heredity
|
November 13, 2010
Genome-wide linkage scan of bipolar disorder in a Colombian population isolate replicates Loci on chromosomes 7p21-22, 1p31, 16p12 and 21q21-22 and identifies a novel locus on chromosome 12q
B Kremeyer, J García, H Müller, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Journal of the Royal Army Medical Corps
|
February 19, 2014
Dieulafoy lesion presenting as severe anaemia in a soldier
Robert M W Burley, I Gavrielides
Annals of Human Genetics
|
November 6, 1998
A mutation screen of the TSC1 gene reveals 26 protein truncating mutations and 1 splice site mutation in a panel of 79 tuberous sclerosis patients
J M Young, M W Burley, S J Jeremiah, et al.
Annals of Human Genetics
|
May 1, 1982
Mapping studies on human mitochondrial glutamate oxaloacetate transaminase
S J Jeremiah, S Povey, M W Burley, et al.
Annals of Human Genetics
|
February 12, 1998
Mapping ESTs to the TSC1 candidate interval by use of the 'Science 96' transcript map
J Wolfe, S Jeremiah, J Young, et al.
Human Immunology
|
June 1, 1989
HLA class III haplotypes in multicase rheumatoid arthritis families
A H Fielder, W Ollier, D K Lord, et al.
Lancet (London, England)
|
July 25, 2000
Non-penetrance in tuberous sclerosis
J P Osborne, A C Jones, M W Burley, et al.
Neurology
|
October 27, 2004
The -1021C->T DBH gene variant is not associated with epilepsy or antiepileptic drug response
C Depondt, H R Cock, D G Healy, et al.
Human Immunology
|
May 1, 1988
C4 complement allotypes in juvenile dermatomyositis
S A Robb, A H Fielder, C E Saunders, et al.
Annals of Human Genetics
|
May 1, 1994
Two loci for tuberous sclerosis: one on 9q34 and one on 16p13
S Povey, M W Burley, J Attwood, et al.
Human Heredity
|
November 13, 2010
Genome-wide linkage scan of bipolar disorder in a Colombian population isolate replicates Loci on chromosomes 7p21-22, 1p31, 16p12 and 21q21-22 and identifies a novel locus on chromosome 12q
B Kremeyer, J García, H Müller, et al.
Page
of 1