1. Genetic Linkage of the Muckle-Wells Syndrome to Chromosome 1q44
Laurence Cuisset, Joost P.H. Drenth, Jean-Marie Berthelot, Alain Meyrier, Gérard Vaudour, Richard A. Watts, David G.I. Scott, Anne Nicholls, Sylvana Pavek, Christian Vasseur, Jacques S. Beckmann, Marc Delpech, Gilles Grateau 
The American Journal of Human Genetics 
Volume 65, Issue 4, Pages (October 1999)
DOI: /302589
Copyright © 1999 The American Society of Human Genetics Terms and Conditions

2. Figure 1
Pedigree of the three families with haplotype analysis in the region of linkage on chromosome 1. Affected individuals are shown as blackened circles (females) or blackened squares (males). Deceased individuals are denoted by diagonal slashes.
The American Journal of Human Genetics  , DOI: ( /302589)
Copyright © 1999 The American Society of Human Genetics Terms and Conditions

3. Figure 2
Multipoint linkage analysis between MWS and selected markers on chromosome 1q. D1S2811 was arbitrarily assigned position 0, and the order and genetic distances of the maker loci were determined by the use of the Généthon genetic map (Dib et al. 1996).
The American Journal of Human Genetics  , DOI: ( /302589)
Copyright © 1999 The American Society of Human Genetics Terms and Conditions