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Mutation Research
|
June 6, 2000
Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factors
C P Daniel, A Fisher, L Parker, et al.
Journal of Medical Genetics
|
March 1, 1995
Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13
S A Lynch, K A Ashcroft, S Zwolinski, et al.
Human Molecular Genetics
|
June 1, 1994
Four novel germ-line mutations in the APC gene detected by heteroduplex analysis
T Hamzehloei, S P West, P D Chapman, et al.
The British Journal of Dermatology
|
May 15, 2020
Detection of genetic tumour predisposition syndromes using electronic health records
S Cook, V Wilson, J Ness, et al.
Annals of Neurology
|
May 13, 1999
The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins
P Piccini, D J Burn, R Ceravolo, et al.
Journal of Chromatography. A
|
June 16, 2001
Experimental studies of uncertainties associated with chromatographic techniques
V J Barwick, S L Ellison, C L Lucking, et al.
Parkinsonism & Related Disorders
|
January 24, 2012
Falling short: underestimation of fracture risk in atypical parkinsonian syndromes
Alison J Yarnall, Gordon W Duncan, Tien K Khoo, et al.
Stroke
|
February 1, 1994
Long-term risk of recurrent stroke after a first-ever stroke. The Oxfordshire Community Stroke Project
J Burn, M Dennis, J Bamford, et al.
Journal of the American Geriatrics Society
|
September 27, 2005
Prevalence and severity of gait disorders in Alzheimer's and non-Alzheimer's dementias
Louise M Allan, Clive G Ballard, David J Burn, et al.
International Journal of Geriatric Psychiatry
|
July 22, 2005
Longitudinal study of cerebral blood flow SPECT in Parkinson's disease with dementia, and dementia with Lewy bodies
Michael J Firbank, David J Burn, Ian G McKeith, et al.
Page
of 57
Search research articles
Search
Showing results (191-200 of 561) with videos related to
Sort By:
Page
of 57
Mutation Research
|
June 6, 2000
Individual variation in somatic mutations of the glycophorin-A gene in neonates in relation to pre-natal factors
C P Daniel, A Fisher, L Parker, et al.
Journal of Medical Genetics
|
March 1, 1995
Kabuki syndrome-like features in monozygotic twin boys with a pseudodicentric chromosome 13
S A Lynch, K A Ashcroft, S Zwolinski, et al.
Human Molecular Genetics
|
June 1, 1994
Four novel germ-line mutations in the APC gene detected by heteroduplex analysis
T Hamzehloei, S P West, P D Chapman, et al.
The British Journal of Dermatology
|
May 15, 2020
Detection of genetic tumour predisposition syndromes using electronic health records
S Cook, V Wilson, J Ness, et al.
Annals of Neurology
|
May 13, 1999
The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins
P Piccini, D J Burn, R Ceravolo, et al.
Journal of Chromatography. A
|
June 16, 2001
Experimental studies of uncertainties associated with chromatographic techniques
V J Barwick, S L Ellison, C L Lucking, et al.
Parkinsonism & Related Disorders
|
January 24, 2012
Falling short: underestimation of fracture risk in atypical parkinsonian syndromes
Alison J Yarnall, Gordon W Duncan, Tien K Khoo, et al.
Stroke
|
February 1, 1994
Long-term risk of recurrent stroke after a first-ever stroke. The Oxfordshire Community Stroke Project
J Burn, M Dennis, J Bamford, et al.
Journal of the American Geriatrics Society
|
September 27, 2005
Prevalence and severity of gait disorders in Alzheimer's and non-Alzheimer's dementias
Louise M Allan, Clive G Ballard, David J Burn, et al.
International Journal of Geriatric Psychiatry
|
July 22, 2005
Longitudinal study of cerebral blood flow SPECT in Parkinson's disease with dementia, and dementia with Lewy bodies
Michael J Firbank, David J Burn, Ian G McKeith, et al.
Page
of 57