[1] Ronchi V.Resolving power of calculated and detected images.J Opt Soc Am,1961,51(4):458~460
[2] Den Dekker A J.van den Bos A.Resolution:a survey.J Opt Soc Am(A),1997,14(3):554~557
[3] Goodman J W.Statistical Optics.Wiley,NewYork,1985:85~88
[4] Fried D L.Resolution,signal-to-noise-ratio,and measurement precision.J Opt Soc Am,1979,69(3):399~406
[5] Fried D L.Resolution,signal-to-noise-ratio,and measurement precision,addendum.J Opt Soc Am,1980,70(6):748~749
[6] Sandison D R,Webb W W.Background rejection and signal-to-noise optimization in confocal and alternativefluorescence microscopes.Applied Optics,1994,33(4):603~615
[7] Rajadhyaksha M,RoxAnderson R,Webb R H.Video-rate confocal scanning laser microscope for imaging human tissues in vivo.Applied OPtics,1999,38(10):2105~2115
[8] Smithepter C L,Dunn A K,Welch A J,et al.Penetration depth limits of in vivo confocal relection imaging.Applied Optics,1998,37(13):2749~2754
[9] Kimura S,Munakata C.Dependence of 3-D optical transfer functions on the pinhole radius in a fluorescent confocal optical microscope.Applied Optics,1990,29(20):3007~3011
[10] Cox I J,Sheppard C J R,Wilson T.Super-resolution by confocal fluorescent microscopy.Optik,1982,60(4):391~396
[11] Kimura S,Munakata C.Calculation of three-dimensional optical transfer function for a confocal scanning fluorescent microscope.J Opt Soc Am.1989,6(7):1015~1019
[12] Nakamura O,Kawata S.Three-dimensional transfer function analysis of the tomographic capalility of a confocal fluorescence micoscope.J Opt Soc Am(A),1990,17(3):522~526