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Neurology|March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene functionM 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 treatmentS 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 concentrationJ A Steele, R A Lewis, M Henini, et al.
Blood|May 16, 1998
Membrane phospholipid asymmetry in human thalassemiaF A Kuypers, J Yuan, R A Lewis, et al.
Diabetes|October 1, 1982
Retinopathy in juvenile-onset type I diabetes of short durationR N Frank, W H Hoffman, M J Podgor, et al.
Ophthalmology|January 1, 1980
Retinopathy in juvenile-onset diabetes of short durationR 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 phenotypeL 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 functionT H Lee, R L Hoover, J D Williams, et al.
Science (New York, N.Y.)|September 22, 2001
Triallelic inheritance in Bardet-Biedl syndrome, a Mendelian recessive disorderN Katsanis, S J Ansley, J L Badano, et al.
Thorax|October 18, 2011
Summary of the British Thoracic Society guidelines for advanced diagnostic and therapeutic flexible bronchoscopy in adultsI A Du Rand, P V Barber, J Goldring, et al.
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