Author/Creator: Nowicki, S. T. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Nowicki, S. T.

1. 127 AN APPROACH TO IDENTIFY EPISTATIC GENES INVOLVED IN THE DEVELOPMENT OF AUTISM SPECTRUM DISORDER IN PATIENTS WITH FRAGILE X SYNDROME. (1st January 2004)

Authors:: Nowicki, S. T.; Jacquemont, S.; Li, L.; Nguyen, D. V.; Gregg, J. P.; Hagerman, R. J.; Hagerman, P. J.; Institute, M. I.N.D.
Journal:: Journal of investigative medicine
Issue:: Volume 52(2004)Supplement 1
Page Start:: S101
Record Type:: Journal Article
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2. 69 THE PRADER-WILLI CLINICAL SUBPHENOTYPE OF FRAGILE X SYNDROME. (1st January 2006)

Authors:: Nowicki, S. T.; Tassone, F.; Ferranti, J.; Ono, M. Y.; Hagerman, R. J.
Journal:: Journal of investigative medicine
Issue:: Volume 54:Number 1(2006)
Page Start:: S91
Record Type:: Journal Article
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