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Journal of Medical Genetics
|
February 1, 1985
Trigonocephaly and the Opitz C syndrome
C Sargent, J Burn, M Baraitser, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 30, 2014
Progression of gait dysfunction in incident Parkinson's disease: impact of medication and phenotype
Brook Galna, Sue Lord, David J Burn, et al.
Journal of Medical Genetics
|
August 1, 1986
Autosomal dominant thoracolaryngopelvic dysplasia: Barnes syndrome
J Burn, C Hall, D Marsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 20, 2003
Central pontine myelinolysis temporally related to hypophosphataemia
A W Michell, D J Burn, P J Reading
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus
|
June 26, 2001
Adenocarcinoma of the rat esophagus in the presence of a proton pump inhibitor: a pilot study
K H Moore, P Barry, J Burn, et al.
Clinical Dysmorphology
|
October 1, 1994
Autosomal dominant transmission of Pallister-Hall syndrome
M Penman Splitt, C Wright, R Perry, et al.
Journal of Medical Genetics
|
October 1, 1993
DiGeorge syndrome: part of CATCH 22
D I Wilson, J Burn, P Scambler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 1994
Differential diagnosis of Parkinson's disease, multiple system atrophy, and Steele-Richardson-Olszewski syndrome: discriminant analysis of striatal 18F-dopa PET data
D J Burn, G V Sawle, D J Brooks
Journal of Medical Genetics
|
June 1, 1984
Orofaciodigital syndrome with mesomelic limb shortening
J Burn, C Dezateux, C M Hall, et al.
Trends in Genetics : TIG
|
October 13, 2009
Detecting new neurodegenerative disease genes: does phenotype accuracy limit the horizon?
David C Samuels, David J Burn, Patrick F Chinnery
Page
of 57
Search research articles
Search
Showing results (131-140 of 561) with videos related to
Sort By:
Page
of 57
Journal of Medical Genetics
|
February 1, 1985
Trigonocephaly and the Opitz C syndrome
C Sargent, J Burn, M Baraitser, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 30, 2014
Progression of gait dysfunction in incident Parkinson's disease: impact of medication and phenotype
Brook Galna, Sue Lord, David J Burn, et al.
Journal of Medical Genetics
|
August 1, 1986
Autosomal dominant thoracolaryngopelvic dysplasia: Barnes syndrome
J Burn, C Hall, D Marsden, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 20, 2003
Central pontine myelinolysis temporally related to hypophosphataemia
A W Michell, D J Burn, P J Reading
Diseases of the Esophagus : Official Journal of the International Society for Diseases of the Esophagus
|
June 26, 2001
Adenocarcinoma of the rat esophagus in the presence of a proton pump inhibitor: a pilot study
K H Moore, P Barry, J Burn, et al.
Clinical Dysmorphology
|
October 1, 1994
Autosomal dominant transmission of Pallister-Hall syndrome
M Penman Splitt, C Wright, R Perry, et al.
Journal of Medical Genetics
|
October 1, 1993
DiGeorge syndrome: part of CATCH 22
D I Wilson, J Burn, P Scambler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 1, 1994
Differential diagnosis of Parkinson's disease, multiple system atrophy, and Steele-Richardson-Olszewski syndrome: discriminant analysis of striatal 18F-dopa PET data
D J Burn, G V Sawle, D J Brooks
Journal of Medical Genetics
|
June 1, 1984
Orofaciodigital syndrome with mesomelic limb shortening
J Burn, C Dezateux, C M Hall, et al.
Trends in Genetics : TIG
|
October 13, 2009
Detecting new neurodegenerative disease genes: does phenotype accuracy limit the horizon?
David C Samuels, David J Burn, Patrick F Chinnery
Page
of 57