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JAMA|October 6, 1993
Rapid fragile X carrier screening and prenatal diagnosis using a nonradioactive PCR testW T Brown, G E Houck, A Jeziorowska, et al.
Clinical Genetics|June 25, 2010
Autism severity is associated with child and maternal MAOA genotypesI L Cohen, X Liu, M E S Lewis, et al.
American Journal of Medical Genetics|July 15, 1994
Fragile X induction systems in CVS cultures: effect on cytogenetic, PCR, and genomic Southern Blot DNA analyses of the FMR-1 geneE C Jenkins, I Morys, J Henderson, et al.
American Journal of Medical Genetics|February 1, 1991
Fragile X screening program in New York StateS L Nolin, D A Snider, E C Jenkins, et al.
STAR Protocols|March 4, 2022
LiverClear: A versatile protocol for mouse liver tissue clearingLaura M Molina, Yekaterina Krutsenko, Nathaniel E C Jenkins, et al.
American Journal of Medical Genetics|April 1, 1992
Mode of inheritance influences behavioral expression and molecular control of cognitive deficits in female carriers of the fragile X syndromeV J Hinton, C S Dobkin, J M Halperin, et al.
Experimental Cell Biology|January 1, 1986
Low frequencies of apparently fragile X chromosomes in normal control cultures: a possible explanationE C Jenkins, W T Brown, J Brooks, et al.
American Journal of Medical Genetics|January 1, 1986
Fragile X and autism: a multicenter surveyW T Brown, E C Jenkins, I L Cohen, et al.
Clinical Genetics|August 1, 1983
Atypical Down syndrome and partial trisomy 21E C Jenkins, C J Duncan, C E Wright, et al.
American Journal of Medical Genetics|May 1, 1988
Recent experience in prenatal fra(X) detectionE C Jenkins, W T Brown, M S Krawczun, et al.
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