Authors:
Ophoff, RA
DeYoung, J
Service, SK
Joose, M
Caffo, NA
Sandkuijl, LA
Terwindt, GM
Haan, J
van den Maagdenberg, AMJM
Jen, J
Baloh, RW
Barilla-LaBarca, ML
Saccone, NL
Atkinson, JP
Ferrari, MD
Freimer, NB
Frants, RR
Citation: Ra. Ophoff et al., Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3, AM J HU GEN, 69(2), 2001, pp. 447-453
Authors:
Taillon-Miller, P
Bauer-Sardina, I
Saccone, NL
Putzel, J
Laitinen, T
Cao, A
Kere, J
Pilia, G
Rice, JP
Kwok, PY
Citation: P. Taillon-miller et al., Juxtaposed regions of extensive and minimal linkage disequilibrium in human Xq25 and Xq28, NAT GENET, 25(3), 2000, pp. 324-328