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Human Genetics|March 1, 1988
DNA linkage analysis of X-linked retinoschisisN Dahl, P Goonewardena, J Chotai, et al.Genomics|February 1, 1988
Linkage analysis of the properdin deficiency gene: suggestion of a locus in the proximal part of the short arm of the X chromosomeP Goonewardena, A G Sjöholm, L A Nilsson, et al.Lancet (London, England)|February 1, 1992
Detection of full fragile X mutationR G Pergolizzi, S H Erster, P Goonewardena, et al.Upsala Journal of Medical Sciences. Supplement|January 1, 1987
DNA studies of X-linked mental retardation associated with a fragile site at Xq27.3P Goonewardena, N Dahl, K H Gustavson, et al.Clinical Genetics|January 1, 1989
Molecular Xp deletion in a male: suggestion of a locus for hypogonadotropic hypogonadism distal to the glycerol kinase and adrenal hypoplasia lociP Goonewardena, N Dahl, M Ritzén, et al.Clinical Genetics|November 1, 1988
A new type of muscular dystrophy in two brothers: analysis by use of DNA probes suggests autosomal recessive inheritanceP Goonewardena, K H Gustavson, I Gamstorp, et al.American Journal of Medical Genetics|April 1, 1992
Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairmentW T Brown, E C Jenkins, P Goonewardena, et al.American Journal of Medical Genetics|February 1, 1991
Detection of fragile X non-penetrant males by DNA marker analysisW T Brown, A Gross, P Goonewardena, et al.Clinical Genetics|October 1, 1986
Analysis of fragile X-mental retardation families using flanking polymorphic DNA probesP Goonewardena, K H Gustavson, G Holmgren, et al.American Journal of Medical Genetics|February 1, 1991
Molecular characterization of a DNA probe, U6.2, located close to the fragile X locusR Pergolizzi, W T Brown, P Goonewardena, et al.Pageof 3