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	1.	Site and sequence specific DNA methylation in the neurofibromatosis (NF1) gene includes C5839T: the site of the recurrent substitution mutation in exon 31. [electronic resource] by Andrews, J D Mancini, D N Singh, S M Rodenhiser, D I Producer: 19961024 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Site-specific DNA methylation in the neurofibromatosis (NF1) promoter interferes with binding of CREB and SP1 transcription factors. [electronic resource] by Mancini, D N Singh, S M Archer, T K Rodenhiser, D I Producer: 19990813 In: Oncogene vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Homonucleotide tracts, short repeats and CpG/CpNpG motifs are frequent sites for heterogeneous mutations in the neurofibromatosis type 1 (NF1) tumour-suppressor gene. [electronic resource] by Rodenhiser, D I Andrews, J D Mancini, D N Jung, J H Singh, S M Producer: 19970321 In: Mutation research vol. 373 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	CpG methylation within the 5' regulatory region of the BRCA1 gene is tumor specific and includes a putative CREB binding site. [electronic resource] by Mancini, D N Rodenhiser, D I Ainsworth, P J O'Malley, F P Singh, S M Xing, W Archer, T K Producer: 19980420 In: Oncogene vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)