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European Journal of Neurology
|
August 11, 2019
Patient-reported outcomes with subcutaneous immunoglobulin in chronic inflammatory demyelinating polyneuropathy: the PATH study
H-P Hartung, R Mallick, V Bril, et al.
American Journal of Medical Genetics
|
March 29, 1996
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)
F Greenberg, R A Lewis, L Potocki, et al.
Science (New York, N.Y.)
|
September 20, 1997
Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration
R Allikmets, N F Shroyer, N Singh, et al.
Human Mutation
|
October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change
K T Hiriyanna, E L Bingham, B M Yashar, et al.
Genetic Epidemiology
|
December 19, 2000
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer
G E Airewele, A J Sigurdson, K J Wiley, et al.
Human Genetics
|
February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America
M T Bassi, A A Bergen, P Bitoun, et al.
Physics in Medicine and Biology
|
October 21, 2005
Dynamic imaging of the lungs using x-ray phase contrast
R A Lewis, N Yagi, M J Kitchen, et al.
American Journal of Human Genetics
|
April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1
I Stoilov, A N Akarsu, I Alozie, et al.
Human Mutation
|
January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies
M M Sohocki, S P Daiger, S J Bowne, et al.
The British Journal of Radiology
|
May 24, 2003
X-ray refraction effects: application to the imaging of biological tissues
R A Lewis, C J Hall, A P Hufton, et al.
Page
of 39
Search research articles
Search
Showing results (351-360 of 381) with videos related to
Sort By:
Page
of 39
European Journal of Neurology
|
August 11, 2019
Patient-reported outcomes with subcutaneous immunoglobulin in chronic inflammatory demyelinating polyneuropathy: the PATH study
H-P Hartung, R Mallick, V Bril, et al.
American Journal of Medical Genetics
|
March 29, 1996
Multi-disciplinary clinical study of Smith-Magenis syndrome (deletion 17p11.2)
F Greenberg, R A Lewis, L Potocki, et al.
Science (New York, N.Y.)
|
September 20, 1997
Mutation of the Stargardt disease gene (ABCR) in age-related macular degeneration
R Allikmets, N F Shroyer, N Singh, et al.
Human Mutation
|
October 26, 1999
Novel mutations in XLRS1 causing retinoschisis, including first evidence of putative leader sequence change
K T Hiriyanna, E L Bingham, B M Yashar, et al.
Genetic Epidemiology
|
December 19, 2000
Neoplasms in neurofibromatosis 1 are related to gender but not to family history of cancer
G E Airewele, A J Sigurdson, K J Wiley, et al.
Human Genetics
|
February 24, 2001
Diverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North America
M T Bassi, A A Bergen, P Bitoun, et al.
Physics in Medicine and Biology
|
October 21, 2005
Dynamic imaging of the lungs using x-ray phase contrast
R A Lewis, N Yagi, M J Kitchen, et al.
American Journal of Human Genetics
|
April 29, 1998
Sequence analysis and homology modeling suggest that primary congenital glaucoma on 2p21 results from mutations disrupting either the hinge region or the conserved core structures of cytochrome P4501B1
I Stoilov, A N Akarsu, I Alozie, et al.
Human Mutation
|
January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies
M M Sohocki, S P Daiger, S J Bowne, et al.
The British Journal of Radiology
|
May 24, 2003
X-ray refraction effects: application to the imaging of biological tissues
R A Lewis, C J Hall, A P Hufton, et al.
Page
of 39