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	661.	Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability. [electronic resource] by Syrrou, M Georgiou, I Paschopoulos, M Lolis, D Producer: 19950802 In: Genetic counseling (Geneva, Switzerland) vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	662.	Modeling of genetic instability--looking for "Newton's binomial" of colon cancer. [electronic resource] by da Costa, Luís Teixeira Producer: 20030616 In: Cancer biology & therapy vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	663.	Bullous ichthyosiform erythroderma, developmental delay, aortic and pulmonary stenosis in association with a FRA12A. [electronic resource] by Berg, J Grace, E Teik, K W Hammond, H Tidman, M FitzPatrick, D Producer: 20001207 In: Clinical dysmorphology vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	664.	FRA3B extends over a broad region and contains a spontaneous HPV16 integration site: direct evidence for the coincidence of viral integration sites and fragile sites. [electronic resource] by Wilke, C M Hall, B K Hoge, A Paradee, W Smith, D I Glover, T W Producer: 19961205 In: Human molecular genetics vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	665.	Fragile X syndrome with extra microchromosome. [electronic resource] by López-Pajares, I Delicado, A Pascual-Castroviejo, I López-Martin, V Moreno, F Garcia-Marcos, J A Producer: 19940921 In: Clinical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	666.	The common fragile site FRA16C does not map within the 16q smallest region of overlap number 2 frequently lost in breast carcinoma. [electronic resource] by Taine, Laurence Rocca-Serra, Philippe El Moneim, Azza Abd Verdier, Nathalie Moradkhani, Kamran Saura, Robert Gorry, Philippe Longy, Michel Bonnet, Françoise Producer: 20030728 In: Cancer genetics and cytogenetics vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	667.	Variant Philadelphia translocations in CML: correlation with fragile sites. [electronic resource] by Sessarego, M Defferrari, R Panarello, C Frassoni, F Mandich, P Ajmar, F Producer: 19880408 In: Cancer genetics and cytogenetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	668.	Further localization of ETS1 indicates that the chromosomal rearrangement in Ewing sarcoma does not occur at fra(11)(q23). [electronic resource] by Simmers, R N Sutherland, G R Producer: 19880323 In: Human genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	669.	Recurrent genomic rearrangements are not at the fragile sites on chromosomes 3 and 5 in human renal cell carcinomas. [electronic resource] by Kovacs, G Brusa, P Producer: 19881019 In: Human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	670.	Absence of significant autosomal lesions in Huntington's disease. [electronic resource] by Beverstock, G C Mol, A Wienhofer, E Producer: 19860109 In: Annals of human genetics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	671.	Mental retardation, megalotestes and a marker X chromosome. [electronic resource] by Fitzsimmons, J McLachlan, J I Fitzsimmons, E Cooke, P Producer: 19820814 In: The Practitioner vol. 226 Availability: No items available. Save to lists Add to cart (remove)
	672.	Prenatal recognition of a defect in DNA repair. [electronic resource] by Hirsch-Kauffmann, M Schweiger, M Producer: 19820521 In: Molecular & general genetics : MGG vol. 184 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	673.	[X chromosome fragility and effects of trimethoprim]. [electronic resource] by Lejeune, J Legrand, N Lafourcade, J Rethoré, M O Raoul, O Maunoury, C Producer: 19821218 In: Annales de genetique vol. 25 Availability: No items available. Save to lists Add to cart (remove)
	674.	Advances in high resolution SIMS studies of BrdU-labelled human metaphase chromosomes. [electronic resource] by Levi-Setti, R Chabala, J M Gavrilov, K Espinosa, R Le Beau, M M Producer: 19961210 In: Cellular and molecular biology (Noisy-le-Grand, France) vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	675.	Links between chromatin structure, DNA repair and chromosome fragility. [electronic resource] by Surrallés, J Puerto, S Ramírez, M J Creus, A Marcos, R Mullenders, L H Natarajan, A T Producer: 19981002 In: Mutation research vol. 404 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	676.	Cancer-specific chromosome alterations in the constitutive fragile region FRA3B. [electronic resource] by Mimori, K Druck, T Inoue, H Alder, H Berk, L Mori, M Huebner, K Croce, C M Producer: 19990719 In: Proceedings of the National Academy of Sciences of the United States of America vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	677.	Aplastic anemia in Nijmegen breakage syndrome. [electronic resource] by Pasic, Srdjan Producer: 20021211 In: The Journal of pediatrics vol. 141 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	678.	Chromosome fragility in dairy cows exposed to dioxins and dioxin-like PCBs. [electronic resource] by Di Meo, G P Perucatti, A Genualdo, V Caputi-Jambrenghi, A Rasero, R Nebbia, C Iannuzzi, L Producer: 20110719 In: Mutagenesis vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	679.	Characterisation of a new rare fragile site easily confused with the fragile X. [electronic resource] by Sutherland, G R Baker, E Producer: 19930528 In: Human molecular genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	680.	Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy. [electronic resource] by Monaco, A P Bertelson, C J Colletti-Feener, C Kunkel, L M Producer: 19870429 In: Human genetics vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 1403 results.