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	861.	Genetic recombination in human melanoma and astrocytoma cell lines involves oncogenes and growth factor genes. [electronic resource] by Lakshmi, M S Sherbet, G V Producer: 19900206 In: Clinical & experimental metastasis vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	862.	Study of a family with a fragile site of the X chromosome at Xq27-28 without mental retardation. [electronic resource] by Voelckel, M A Philip, N Piquet, C Pellissier, M C Oberlé, I Birg, F Mattei, M G Mattei, J F Producer: 19890512 In: Human genetics vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	863.	Variability in expression of common fragile sites: in search of a new criterion. [electronic resource] by Jordan, D K Burns, T L Divelbiss, J E Woolson, R F Patil, S R Producer: 19901205 In: Human genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	864.	Autism and the fragile X syndrome. [electronic resource] by Fisch, G S Cohen, I L Wolf, E G Brown, W T Jenkins, E C Gross, A Producer: 19860205 In: The American journal of psychiatry vol. 143 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	865.	DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes. [electronic resource] by Glover, T W Berger, C Coyle, J Echo, B Producer: 19840919 In: Human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	866.	The expression of common fragile sites in peripheral blood lymphocytes of breast and colorectal cancer patients with aphidicolin. [electronic resource] by Balci, A Ekmekci, A Cetin, R Producer: 20000621 In: The Tohoku journal of experimental medicine vol. 189 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	867.	Assignment of FRA1H common fragile site to human chromosome band 1q42.1 proximal to the nuclear NAD+ ADP-ribosyltransferase gene (ADPRT) and to the main 5S rRNA gene locus. [electronic resource] by Pelliccia, F Limongi, M Z Gaddini, L Rocchi, A Producer: 19981106 In: Cytogenetics and cell genetics vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	868.	Recurrent chromosomal rearrangements involving breakpoints 3p21 and 19q13 in Chinese IgD multiple myeloma detected by G-banding and multicolor spectral karyotyping: a review of IgD karyotype literature. [electronic resource] by Ng, M H Wong, N Tsang, K S Cheng, S H Chung, Y F Lo, K W Producer: 20011018 In: Human pathology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	869.	Chromosomal defects in 34 male homosexuals, half of them with HIV antibodies. [electronic resource] by Castro-Volio, Isabel Valle-Bourrette, Luisa Producer: 20021220 In: Revista de biologia tropical vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	870.	Replication dynamics at common fragile site FRA6E. [electronic resource] by Palumbo, Elisa Matricardi, Laura Tosoni, Elena Bensimon, Aaron Russo, Antonella Producer: 20110222 In: Chromosoma vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	871.	Autosomal folate sensitive fragile sites in normal and mentally retarded individuals in Greece. [electronic resource] by Mavrou, A Syrrou, M Tsenghi, C Metaxotou, C Producer: 19910521 In: American journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	872.	Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site. [electronic resource] by Mattei, M G Baeteman, M A Heilig, R Oberlé, I Davies, K Mandel, J L Mattei, J F Producer: 19850530 In: Human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	873.	Major histocompatibility complex, t-complex, and leukemia. [electronic resource] by Dorak, M T Burnett, A K Producer: 19920730 In: Cancer causes & control : CCC vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	874.	Clustering of C2-H2 zinc finger motif sequences within telomeric and fragile site regions of human chromosomes. [electronic resource] by Lichter, P Bray, P Ried, T Dawid, I B Ward, D C Producer: 19920922 In: Genomics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	875.	Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions. [electronic resource] by Wang, L Paradee, W Mullins, C Shridhar, R Rosati, R Wilke, C M Glover, T W Smith, D I Producer: 19970701 In: Genomics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	876.	Characterization of the common fragile site FRA9E and its potential role in ovarian cancer. [electronic resource] by Callahan, Gwen Denison, Stacy R Phillips, Leslie A Shridhar, Viji Smith, David I Producer: 20030212 In: Oncogene vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	877.	Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage. [electronic resource] by Jones, C Müllenbach, R Grossfeld, P Auer, R Favier, R Chien, K James, M Tunnacliffe, A Cotter, F Producer: 20000623 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	878.	Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies. [electronic resource] by Lavanchy, L Munier, F L Cousin, P Gaide, A C Thonney, F Schorderet, D F Producer: 20010621 In: Ophthalmic genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	879.	Trinucleotide repeats and other microsatellites in yeasts. [electronic resource] by Richard, G F Hennequin, C Thierry, A Dujon, B Producer: 20000301 In: Research in microbiology vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	880.	Loss of Ubr2, an E3 ubiquitin ligase, leads to chromosome fragility and impaired homologous recombinational repair. [electronic resource] by Ouyang, Yan Kwon, Yong Tae An, Jee Young Eller, Danny Tsai, Shih-Chang Diaz-Perez, Silvia Troke, Joshua J Teitell, Michael A Marahrens, York Producer: 20060705 In: Mutation research vol. 596 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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