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Lancet (London, England)|February 1, 1992
Detection of full fragile X mutationR G Pergolizzi, S H Erster, P Goonewardena, et al.Human Genetics|September 1, 1992
Polymerase chain reaction analysis of fragile X mutationsS H Erster, W T Brown, P Goonewardena, et al.Molecular and Chemical Neuropathology|February 1, 1994
Analysis of chromosome 22 loci in meningioma. Alterations in the leukemia inhibitory factor (LIF) locusR G Pergolizzi, S H ErsterAmerican Journal of Human Genetics|December 1, 1993
Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general populationK Snow, L K Doud, R Hagerman, 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.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.American Journal of Medical Genetics|February 1, 1991
Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8W T Brown, A C Gross, P Goonewardena, et al.Cancer Letters|February 1, 1980
The effect of exogenous nutrients on the biosynthesis of Y base in tRNAPHe from Ehrlich ascites carcinomaR G Pergolizzi, D GrunbergerGenomics|April 1, 1992
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28G G Consalez, C L Stayton, N B Freimer, et al.Pageof 22