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Peters' anomaly is usually a sporadic or autosomal recessive condition. We present three families whose members had dominantly inherited anterior segment anomalies with variable expression, including typical Peters' anomaly in at least one family member. Slit-lamp examination of parents and family members of children with Peters' anomaly is therefore important to exclude dominant inheritance.

Aaron Reid In his short story “The Rich Brother” Tobias Wolff delineates a tale of two brothers who have many external differences resulting from their differences in faith. The two brothers are Pete and Donald, and they live in present day California, where their lives are much different from each other. Pete owns a Century 21 franchise and has a wife and two children, and many highly regarded...

Quantified sentences constitute a recalcitrant problem for theories of presupposition projection, and a great number of attempts have been made to explicate the projection properties of quantificational expressions (Karttunen & Peters 1979, Cooper 1983, Heim 1983, van der Sandt 1992, Beaver 1994, 2001, Fox 2008, 2012, George 2008a,b, Schlenker 2008, Charlow 2009, Chemla 2009b, Schlenker 2009, F...

Carleton, A. B., Peters, R. A., Stocken, L. A., Thompson, R. H. S. & Williams, D. I.; appendix by Storey, I. D. E., Levvy, G. A. & Chance, A. C. (1944). Interim Report to Medical Research Council. Eagle, H. (1943). By communication.* Eagle, H. (1944). By communication.* Longcope, W. T., Wintrobe, M. M. & Luetscher, J. A. (1943). By communication.* Peters, R. A. (1921). J. Phy8iol. 55, 1. Peters...

Recently introduced versions of the Borsuk-Ulam theorem (BUT) state that a feature on a n-manifold projects to two features with matching description onto a n+1 manifold (Peters, 2016; Peters and Tozzi, 2016a, 2016b; Tozzi, 2016; Tozzi and Peters, 2016a, 2016b). Starting from this rather simple “abstract” claim, a fruitful general framework has been built, able to elucidate disparate “real” phy...

BACKGROUND Peters Plus syndrome (MIM 261540) is a rare autosomal recessive condition characterized by ocular defects (typically Peters anomaly) and other systemic major/minor abnormalities. Mutations in the B3GALTL gene encoding the β-1,3-glucosyltransferase have been found in virtually all patients with typical Peters Plus syndrome. CASE PRESENTATION We report here a female patient with seve...