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American Journal of Human Genetics
|
April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia
B A Bejjani, R A Lewis, K F Tomey, et al.
Human Molecular Genetics
|
October 9, 2001
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations
S Aradhya, H Woffendin, T Jakins, et al.
Neurology
|
March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene function
M E Shy, C Siskind, E R Swan, et al.
Ophthalmology
|
January 1, 1989
A comparison of the ocular hypotensive efficacy of once-daily and twice-daily levobunolol treatment
S I Rakofsky, S Melamed, J S Cohen, et al.
Optics Express
|
June 13, 2014
Raman scattering reveals strong LO-phonon-hole-plasmon coupling in nominally undoped GaAsBi: optical determination of carrier concentration
J A Steele, R A Lewis, M Henini, et al.
Blood
|
May 16, 1998
Membrane phospholipid asymmetry in human thalassemia
F A Kuypers, J Yuan, R A Lewis, et al.
Diabetes
|
October 1, 1982
Retinopathy in juvenile-onset type I diabetes of short duration
R N Frank, W H Hoffman, M J Podgor, et al.
Ophthalmology
|
January 1, 1980
Retinopathy in juvenile-onset diabetes of short duration
R N Frank, W H Hoffman, M J Podgor, et al.
American Journal of Human Genetics
|
December 1, 1994
Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype
L R Weitkamp, A J Moss, R A Lewis, et al.
The New England Journal of Medicine
|
May 9, 1985
Effect of dietary enrichment with eicosapentaenoic and docosahexaenoic acids on in vitro neutrophil and monocyte leukotriene generation and neutrophil function
T H Lee, R L Hoover, J D Williams, et al.
Page
of 39
Search research articles
Search
Showing results (331-340 of 381) with videos related to
Sort By:
Page
of 39
American Journal of Human Genetics
|
April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi Arabia
B A Bejjani, R A Lewis, K F Tomey, et al.
Human Molecular Genetics
|
October 9, 2001
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutations
S Aradhya, H Woffendin, T Jakins, et al.
Neurology
|
March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene function
M E Shy, C Siskind, E R Swan, et al.
Ophthalmology
|
January 1, 1989
A comparison of the ocular hypotensive efficacy of once-daily and twice-daily levobunolol treatment
S I Rakofsky, S Melamed, J S Cohen, et al.
Optics Express
|
June 13, 2014
Raman scattering reveals strong LO-phonon-hole-plasmon coupling in nominally undoped GaAsBi: optical determination of carrier concentration
J A Steele, R A Lewis, M Henini, et al.
Blood
|
May 16, 1998
Membrane phospholipid asymmetry in human thalassemia
F A Kuypers, J Yuan, R A Lewis, et al.
Diabetes
|
October 1, 1982
Retinopathy in juvenile-onset type I diabetes of short duration
R N Frank, W H Hoffman, M J Podgor, et al.
Ophthalmology
|
January 1, 1980
Retinopathy in juvenile-onset diabetes of short duration
R N Frank, W H Hoffman, M J Podgor, et al.
American Journal of Human Genetics
|
December 1, 1994
Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype
L R Weitkamp, A J Moss, R A Lewis, et al.
The New England Journal of Medicine
|
May 9, 1985
Effect of dietary enrichment with eicosapentaenoic and docosahexaenoic acids on in vitro neutrophil and monocyte leukotriene generation and neutrophil function
T H Lee, R L Hoover, J D Williams, et al.
Page
of 39