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The New Zealand Medical Journal
|
May 24, 1989
Chronic paroxysmal hemicrania
J C MacMillan, H Nukada
Clinical Genetics
|
October 1, 1992
The Charcot-Marie-Tooth syndrome: perceptions of disability and projected use of DNA diagnostic tests
J C MacMillan, P S Harper
Annals of Neurology
|
September 1, 1991
Single-gene neurological disorders in South Wales: an epidemiological study
J C MacMillan, P S Harper
Clinical Genetics
|
March 1, 1994
The Charcot-Marie-Tooth syndrome: clinical aspects from a population study in South Wales, UK
J C MacMillan, P S Harper
Bailliere'S Clinical Gastroenterology
|
January 16, 1999
Arteriohepatic dysplasia (Alagille syndrome; Watson-Alagille syndrome)
J C MacMillan, R Shepherd, M Heritage
Canadian Family Physician Medecin De Famille Canadien
|
January 27, 2011
Help for the chemically dependent physician: a treatment program and its outcomes
J G Macdonald, J C Macmillan, D Harris
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1995
Molecular diagnostic analysis for Huntington's disease: a prospective evaluation
J C MacMillan, P Davies, P S Harper
Journal of Medical Genetics
|
January 1, 1992
Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families
J C MacMillan, M Upadhyaya, P S Harper
The Journal of Thoracic and Cardiovascular Surgery
|
May 1, 1978
Clinical spectrum of septic pulmonary embolism and infarction
J C MacMillan, S H Milstein, P C Samson
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
September 2, 2003
Adult onset Krabbe disease may mimic motor neurone disease
R D Henderson, J C MacMillan, J M Bradfield
Page
of 4
Search research articles
Search
Showing results (1-10 of 34) with videos related to
Sort By:
Page
of 4
The New Zealand Medical Journal
|
May 24, 1989
Chronic paroxysmal hemicrania
J C MacMillan, H Nukada
Clinical Genetics
|
October 1, 1992
The Charcot-Marie-Tooth syndrome: perceptions of disability and projected use of DNA diagnostic tests
J C MacMillan, P S Harper
Annals of Neurology
|
September 1, 1991
Single-gene neurological disorders in South Wales: an epidemiological study
J C MacMillan, P S Harper
Clinical Genetics
|
March 1, 1994
The Charcot-Marie-Tooth syndrome: clinical aspects from a population study in South Wales, UK
J C MacMillan, P S Harper
Bailliere'S Clinical Gastroenterology
|
January 16, 1999
Arteriohepatic dysplasia (Alagille syndrome; Watson-Alagille syndrome)
J C MacMillan, R Shepherd, M Heritage
Canadian Family Physician Medecin De Famille Canadien
|
January 27, 2011
Help for the chemically dependent physician: a treatment program and its outcomes
J G Macdonald, J C Macmillan, D Harris
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1995
Molecular diagnostic analysis for Huntington's disease: a prospective evaluation
J C MacMillan, P Davies, P S Harper
Journal of Medical Genetics
|
January 1, 1992
Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families
J C MacMillan, M Upadhyaya, P S Harper
The Journal of Thoracic and Cardiovascular Surgery
|
May 1, 1978
Clinical spectrum of septic pulmonary embolism and infarction
J C MacMillan, S H Milstein, P C Samson
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia
|
September 2, 2003
Adult onset Krabbe disease may mimic motor neurone disease
R D Henderson, J C MacMillan, J M Bradfield
Page
of 4