Localization of PGL1 by recombinant and haplotype analyses in families

pgl1map2.gif (9679 bytes)
Data compiled from Van Schothorst et al. (1996, 1998), Baysal et al. (1997, 1999)


References

Baysal BE, Farr JE, Rubinstein WS, Galus RA, Johnson KA, Aston CE, Myers EN, Johnson JT, Carrau R, Kirkpatrick SJ, Myssiorek D, Singh D, Saha S, Gollin SM, Evans GA, James MR, Richard CW (1997) Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23. Am J Hum Genet, 60: 121-132.

Baysal BE, Van Schothorst EM, Farr JE, Grashof P, Myssiorek D, Rubinstein WS, Taschner P, Cornelisse CJ, Devlin B, Devilee P, Richard CW (1999) Repositioning the hereditary paraganglioma critical region on chromosome band 11q23. Hum Genet, 104: 219-225.

Van Schothorst EM, Jansen JC, Bardoel A, Van der Mey AGL, James MJ, Sobol H, Weissenbach J, Van Ommen G-JB, Cornelisse CJ, Devilee P (1996) Confinement of PGL, an imprinted gene causing hereditary paragangliomas, to a 2 cM interval on 11q22-q23 and exclusion of DRD2 and NCAM as candidate genes. Eur J Hum Genet, 4: 267-273.

Van Schothorst EM, Jansen JC, Grooters E, Prins DEM, Wiersinga LJ, Van der Mey AGL, Van Ommen G-JB, Devilee P, Cornelisse CJ (1998) Founder effect at PGL1 in hereditary head and neck paraganglioma families from The Netherlands. Am J Hum Genet, 63: 468-473.