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American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: linkage analysis in black and white populationsC E Schwartz, M C Phelan, C Brightharp, et al.Biochemical and Biophysical Research Communications|October 30, 1986
Localization of a human gene homologous to the PrP gene on the p arm of chromosome 20 and detection of PrP-related antigens in normal human brainN K Robakis, E A Devine-Gage, E C Jenkins, et al.Clinical Oncology (Royal College of Radiologists (Great Britain))|August 18, 2009
Application of robotic stereotactic radiotherapy to peripheral stage I non-small cell lung cancer with curative intentW T Brown, X Wu, F Fayad, et al.Annals of Neurology|December 1, 1985
Fragile X syndrome: associated neurological abnormalities and developmental disabilitiesK E Wisniewski, J H French, S Fernando, 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.American Journal of Mental Retardation : AJMR|March 1, 1988
Social gaze, social avoidance, and repetitive behavior in fragile X males: a controlled studyI L Cohen, G S Fisch, V Sudhalter, et al.American Journal of Medical Genetics|July 12, 1996
Fragile X founder effects and new mutations in FinlandN Zhong, E Kajanoja, B Smits, et al.Journal of Genetic Counseling|November 16, 2013
Molecular carrier testing for the fragile X syndrome: Issues for genetic counselorsJ L Berliner, F N Shapiro, S L Nolin, et al.American Journal of Human Genetics|October 1, 1993
Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndromeA McConkie-Rosell, A M Lachiewicz, G A Spiridigliozzi, et al.American Journal of Human Genetics|August 27, 1998
Examination of factors associated with instability of the FMR1 CGG repeatA E Ashley-Koch, H Robinson, A E Glicksman, et al.Pageof 23