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Nucleic Acids Research
|
August 11, 1988
A chromosome 1 BglI RFLP for the LR67 anonymous DNA segment [D1S26]
L R Griffiths, D A Ross, N Mesterovic, et al.
Muscle & Nerve
|
February 18, 1998
Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1)
S Sander, G A Nicholson, R A Ouvrier, et al.
Nature Genetics
|
March 10, 2001
Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
J L Dawkins, D J Hulme, S B Brahmbhatt, et al.
Neuroscience Letters
|
July 26, 1996
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients
E Bellone, A Schenone, G Mancardi, et al.
Neurology
|
August 10, 2005
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations
D Zhu, M L Kennerson, G Walizada, et al.
Australian and New Zealand Journal of Medicine
|
October 1, 1996
Apolipoprotein E genotyping in Alzheimer's disease in an Australian sample
J G Yang, R A Poropat, W S Brooks, et al.
Neurology
|
February 1, 1989
Heterogeneity evidence and linkage studies on Charcot-Marie-Tooth disease
L R Griffiths, M B Zwi, J G McLeod, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery
|
August 22, 2014
A national trainee-led audit of inguinal hernia repair in Scotland
S O'Neill, A G Robertson, A J Robson, et al.
Clinical Genetics
|
December 15, 2015
Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies
S Tey, A Ahmad-Annuar, A P Drew, et al.
The New England Journal of Medicine
|
November 14, 1991
Undertreatment of glaucoma among black Americans
J C Javitt, A M McBean, G A Nicholson, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 115) with videos related to
Sort By:
Page
of 12
Nucleic Acids Research
|
August 11, 1988
A chromosome 1 BglI RFLP for the LR67 anonymous DNA segment [D1S26]
L R Griffiths, D A Ross, N Mesterovic, et al.
Muscle & Nerve
|
February 18, 1998
Charcot-Marie-Tooth disease: histopathological features of the peripheral myelin protein (PMP22) duplication (CMT1A) and connexin32 mutations (CMTX1)
S Sander, G A Nicholson, R A Ouvrier, et al.
Nature Genetics
|
March 10, 2001
Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain base subunit-1, cause hereditary sensory neuropathy type I
J L Dawkins, D J Hulme, S B Brahmbhatt, et al.
Neuroscience Letters
|
July 26, 1996
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patients
E Bellone, A Schenone, G Mancardi, et al.
Neurology
|
August 10, 2005
Charcot-Marie-Tooth with pyramidal signs is genetically heterogeneous: families with and without MFN2 mutations
D Zhu, M L Kennerson, G Walizada, et al.
Australian and New Zealand Journal of Medicine
|
October 1, 1996
Apolipoprotein E genotyping in Alzheimer's disease in an Australian sample
J G Yang, R A Poropat, W S Brooks, et al.
Neurology
|
February 1, 1989
Heterogeneity evidence and linkage studies on Charcot-Marie-Tooth disease
L R Griffiths, M B Zwi, J G McLeod, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery
|
August 22, 2014
A national trainee-led audit of inguinal hernia repair in Scotland
S O'Neill, A G Robertson, A J Robson, et al.
Clinical Genetics
|
December 15, 2015
Mutation analysis of genes within the dynactin complex in a cohort of hereditary peripheral neuropathies
S Tey, A Ahmad-Annuar, A P Drew, et al.
The New England Journal of Medicine
|
November 14, 1991
Undertreatment of glaucoma among black Americans
J C Javitt, A M McBean, G A Nicholson, et al.
Page
of 12