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American Journal of Medical Genetics. Supplement|January 1, 1986
Chromosome findings in the Rett syndrome and a test of a two-step mutation theoryJ Wahlström, M AnvretAmerican Journal of Medical Genetics|September 1, 1990
Segregation analysis of the X-chromosome in a family with Rett syndrome in two generationsM Anvret, J Wahlström, P Skogsberg, et al.Brain & Development|January 1, 1985
Linkage analysis of the Rett syndrome using human chromosomal specific probesM Anvret, I M Johansson, J Wahlström, et al.Clinical Genetics|October 1, 1988
Infantile autism, fragile (X) (q27.3) and RFLP analysis in an extended Swedish familyM Anvret, C Gillberg, J Wahlström, et al.Brain & Development|January 1, 1990
The Rett syndrome related to fragile X(P22) in caffeine-induced lymphocyte cultureJ Wahlström, I Witt-Engerström, L Mellquist, et al.Clinical Genetics|November 1, 1987
Linkage of G8 (D4S10) in two Swedish families with Huntington's diseaseG Holmgren, E W Almqvist, M Anvret, et al.Biochemical and Biophysical Research Communications|February 13, 1997
Characterization and regulation of the nonerythroid porphobilinogen deaminase promoterG Lundin, M AnvretPageof 26