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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.
Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1991
Evaluation of DNA-based diagnosis for haemophilia AC Wadelius, M Blombäck, P Goonewardena, et al.
Clinical Genetics|June 1, 1988
A linkage study of the locus for X-linked Charcot-Marie-Tooth diseaseP Goonewardena, J Welihinda, M Anvret, et al.
Clinical Genetics|December 1, 1991
Genetic mapping of loci for X-linked retinitis pigmentosaN Dahl, M Sundvall, U Pettersson, et al.
Human Genetics|September 1, 1992
Polymerase chain reaction analysis of fragile X mutationsS H Erster, W T Brown, P Goonewardena, et al.
American Journal of Human Genetics|August 1, 1989
Linkage analysis of families with fragile-X mental retardation, using a novel RFLP marker (DXS 304)N Dahl, P Goonewardena, H Malmgren, et al.
Human Genetics|June 1, 1989
Isolation of a DNA probe of potential use for diagnosis of the fragile-X syndromeN Dahl, K Hammarström-Heeroma, P Goonewardena, et al.
Genomics|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.
Nature Genetics|July 1, 1992
Evidence of founder chromosomes in fragile X syndromeR I Richards, K Holman, K Friend, et al.
American Journal of Medical Genetics|February 1, 1991
Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304P Goonewardena, W T Brown, A C Gross, et al.
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