A search for rhenium lines in the Fraunhofer spectrum von Swensson, J. W.

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Comments on forbidden sulphur I lines in the solar spectrum von Swensson, J. W.

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The Spectrum of Procyon: a Typical Star of Class F von Swensson, J. W.

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Forbidden lines of neutral carbon in the solar spectrum von Swensson, J. W.

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Structures of neutral manganese lines in the infrared solar spectrum von Swensson, J. W.

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The Spectrum Variable ∊ Ursae Majoris von Swensson, J. W.

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BD+14°3887, a Peculiar be Star Showing Emission Lines of Nα i, [Fe III], and he i; with a Note on the Spectrum of CD-27°11944 von Swensson, J. W.

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HYPERFINE STRUCTURE OF MN I LINES IN THE SOLAR SPECTRUM. PHOSPHORUS LINES IN THE SOLAR SPECTRUM von Swensson, J. W

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MG I LINES IN THE SOLAR SPECTRUM von Swensson,J. W, Risberg,G

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Les spectres de treize nébuleuses planétaires et de leurs noyaux von Swings, Polydore, Swensson, J.-W.

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The Spectrum of Doubly Ionized Titanium, Ti III von Edlén, Bengt, Swensson, John W

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IV. The Abundances of the Chemical Elements in the Universe von Struve, Otto, Swensson, J. W., Minnaert, M.

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NITROGEN LINES IN THE INFRARED FRAUNHOFER SPECTRUM. THE SOLAR SPECTRUM IN THE 5577 AND 6300 A REGIONS von Swensson,J. W, Roland,G, Delbouille,L

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The Solar Spectrum From Lambda 7498 to Lambda 12016: A Table of Measures and Identifications von Swensson,J. W, Benedict,W. S, Delbouille,L, Roland,G

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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy von Irvine, Alan D, Corden, Laura D, Swensson, Ole, Swensson, Beate, Moore, Jonathan E, Frazer, David G, Smith, Frances J.D, Knowlton, Robert G, Christophers, Enno, Rochels, Rainer, Uitto, Jouni, McLean, W.H. Irwin

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New models and online calculator for predicting non-sentinel lymph node status in sentinel lymph node positive breast cancer patients von Kohrt, Holbrook E, Olshen, Richard A, Bermas, Honnie R, Goodson, William H, Wood, Douglas J, Henry, Solomon, Rouse, Robert V, Bailey, Lisa, Philben, Vicki J, Dirbas, Frederick M, Dunn, Jocelyn J, Johnson, Denise L, Wapnir, Irene L, Carlson, Robert W, Stockdale, Frank E, Hansen, Nora M, Jeffrey, Stefanie S

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Molecular Genetics of Meesmann's Corneal Dystrophy: Ancestral and Novel Mutations in Keratin 12 (K12) and Complete Sequence of the Human KRT12 Gene von CORDEN, LAURA D., SWENSSON, OLE, SWENSSON, BEATE, SMITH, FRANCES J.D., ROCHELS, RAINER, UITTO, JOUNI, McLEAN, W.H.IRWIN

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Keratin 16 and keratin 17 mutations cause pachyonychia congenita von McLean, W.H.I, Rugg, E.L, Lunny, D.P, Morley, S.M, Lane, E.B, Swensson, O, Dopping-Hepenstal, P.J.C, Griffiths, W.A.D, Eady, R.A.J, Higgins, C, Navsaria, H.A, Leigh, I.M, Strachan, T, Kunkeler, L, Munro, C.S

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Specialized keratin expression pattern in human ridged skin as an adaptation to high physical stress von SWENSSON, O, LANGBEIN, L, MCMILLAN, J. R, STEVENS, H. P, LEIGH, I. M, MCLEAN, W. H. I, LANE, E. B, EADY, R. A. J

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A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy von Corden, L D, Swensson, O, Swensson, B, Rochels, R, Wannke, B, Thiel, H J, McLean, W H I

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