Closed-end country funds can trade at large premiums and discounts from their foreign
asset values (NAVs). Investigating this anomaly, we find that individual fund premiums move …

The predominantly autosomal dominant disorder, oculodentodigital dysplasia (ODDD) has
high penetrance with intra‐ and interfamilial phenotypic variability. Abnormalities observed in …

… Bodurtha acknowledges financial support from a University of Michigan School of Business
summer grant and Citicorp, NA All errors are our own.Search for more papers by this author …

Method The authors conducted semistructured interviews with Johns Hopkins University
School of Medicine faculty in 2016: department chairs (sponsors) and faculty participants of an …

Purpose This study characterizes the US clinical genetics workforce to inform workforce
planning and public policy development. Methods A 32-question survey was electronically …

A range of phenotypes including Greig cephalopolysyndactyly and Pallister‐Hall syndromes
(GCPS, PHS) are caused by pathogenic mutation of the GLI3 gene. To characterize the …

Applying Fishburn's [4] conditions for convex stochastic dominance, exact linear programming
algorithms are proposed and implemented for assigning discrete return distributions into …

Coffin–Siris syndrome (CSS) is a rare, clinically heterogeneous disorder often considered in
the setting of cognitive/developmental delay and 5th finger/nail hypoplasia. Due to the …

… Cho is grateful for the summer research support provided by the School of Business, and
Bodurtha received research support from Citicorp, NA and a University of Michigan School of …

Null mutations in cartilage-associated protein (CRTAP) and prolyl 3-hydroxylase 1 (P3H1/LEPRE1)
cause types VII and VIII OI, respectively, two novel recessive forms of osteogenesis …