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American Journal of Medical Genetics|July 23, 1998
Normal adaptive function with learning disability in duplication 8p including band p22S S Sklower Brooks, M Genovese, H Gu, et al.European Journal of Medical Genetics|June 15, 2005
Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotypeM Velinov, J Kupferman, H Gu, et al.American Journal of Medical Genetics|February 1, 1991
Distribution of diploidy, polyploidy, and endoreduplication in fra(X) positive and negative lymphocytes, amniocytes, and chorionic villiE C Jenkins, M M Sanz, J H Ray, et al.American Journal of Medical Genetics|April 1, 1992
Prenatal detection of fra(X)(q27.3) in female identical twins: reliability of low level cytogenetic prenatal expression in femalesE C Jenkins, W T Brown, S Schonberg, et al.Human Genetics|September 1, 1992
Polymerase chain reaction analysis of fragile X mutationsS H Erster, W T Brown, P Goonewardena, et al.The American Journal of Psychiatry|January 1, 1986
Autism and the fragile X syndromeG S Fisch, I L Cohen, E G Wolf, et al.American Journal of Medical Genetics|February 11, 1997
Transmission electron microscopy of chromosomes by longitudinal section preparation: application to fragile X chromosome analysisG Y Wen, E C Jenkins, X L Yao, et al.Neuropsychologia|January 1, 1986
A profile of cognitive deficit in females from fragile X familiesC M Miezejeski, E C Jenkins, A L Hill, et al.American Journal of Medical Genetics|May 1, 1988
Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile XW T Brown, W Ye, A C Gross, et al.American Journal of Medical Genetics|April 20, 1999
Ultrastructure of the fragile X chromosome: new observations on the fragile siteG Y Wen, E C Jenkins, E M Goldberg, et al.Pageof 12