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American Journal of Medical Genetics|January 1, 1986
DNA linkage studies in the fragile X syndrome suggest genetic heterogeneityW T Brown, A C Gross, C B Chan, et al.American Journal of Medical Genetics|May 1, 1988
Fragile X expression in short-term whole blood cultures is affected by cell densityM S Krawczun, E C Jenkins, W T Brown, et al.Metabolism: Clinical and Experimental|August 1, 1997
Response to nutritional and growth hormone treatment in progeriaJ E Abdenur, W T Brown, S Friedman, et al.Protein Expression and Purification|May 25, 1999
An Escherichia coli expression vector that allows recovery of proteins with native N-termini from purified calmodulin-binding peptide fusionsD L Wyborski, J C Bauer, C F Zheng, et al.Journal of Medical Genetics|October 1, 1990
Monozygotic twins with trisomy 18: a report of discordant phenotypeJ S Schlessel, W T Brown, A Lysikiewicz, et al.Neurogenetics|February 7, 2001
5-HTTLPR variants not associated with autistic spectrum disordersN Zhong, L Ye, W Ju, et al.American Journal of Medical Genetics|August 9, 1996
Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypesN Zhong, W Ju, J Pietrofesa, et al.Molecular Genetics and Metabolism|February 3, 2000
The feasibility of PCR-based diagnosis of Prader-Willi and Angelman syndromes using restriction analysis after bisulfite modification of genomic DNAM Velinov, H Gu, M Genovese, et al.Neuroscience|September 29, 2000
Fmr1 knockout mouse has a distinctive strain-specific learning impairmentC Dobkin, A Rabe, R Dumas, et al.American Journal of Medical Genetics|April 1, 1992
Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairmentW T Brown, E C Jenkins, P Goonewardena, et al.Pageof 23