Your search returned 1403 results.

Results
	461.	The genetic toxicology of 5-bromodeoxyuridine in mammalian cells. [electronic resource] by Morris, S M Producer: 19910930 In: Mutation research vol. 258 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	462.	Progress toward an internal control system for fragile-X induction by 5-fluorodeoxyuridine in whole-blood cultures. [electronic resource] by Jenkins, E C Duncan, C J Sanz, M M Genovese, M Gu, H Schwartz-Richstein, C Lele, K P Salandi, M L Krawczun, M S Producer: 19910122 In: Pathobiology : journal of immunopathology, molecular and cellular biology vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	463.	Expression of the autosomal folate-sensitive fragile sites in ten kindreds with Martin-Bell syndrome. [electronic resource] by Ventruto, V Stabile, M Gentile, G de Tollis, G Colantuoni, M Sirone, P Perone, L Lonardo, F Della Monica, M Fiore, M Producer: 19860701 In: Annales de genetique vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	464.	Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23. [electronic resource] by Voullaire, L E Webb, G C Leversha, M A Producer: 19870901 In: Human genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	465.	Fra(X)(p22) not associated with infantile autism. [electronic resource] Producer: 19850117 In: Lancet (London, England) vol. 2 Availability: No items available. Save to lists Add to cart (remove)
	466.	An in vitro and in vivo study of a BrdU-sensitive fragile site in the Chinese hamster. [electronic resource] by Lin, M S Takabayashi, T Wilson, M G Marchese, C A Producer: 19841128 In: Cytogenetics and cell genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	467.	Behavior of chromosome cores at heritable fragile sites: 16q22 and Xq27. [electronic resource] by Howard-Peebles, P N Howell, W M Producer: 19820225 In: Cytogenetics and cell genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	468.	Chromosomes, genes, and cancer breakpoints. [electronic resource] by Musio, Antonio Zambroni, Desirée Vezzoni, Paolo Mariani, Tullio Producer: 20030224 In: Cancer genetics and cytogenetics vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	469.	Testing the nonrandomness of chromosomal breakpoints using highest observed breakages. [electronic resource] by Hou, C D Chiang, J Tai, J J Producer: 19990625 In: Human genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	470.	New gene forges link between fragile site and many cancers. [electronic resource] by Pennisi, E Producer: 19960606 In: Science (New York, N.Y.) vol. 272 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	471.	Translocation (1;5)(q32;q35) in CD30+ anaplastic large cell non-Hodgkin lymphona of childhood. A case report. [electronic resource] by Tone, L G Defavery, R Scrideli, C A Bernardes, J E Torres, F M Soares, F A Peres, L C Duarte, M H Producer: 19960610 In: Cancer genetics and cytogenetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	472.	Normal expression of fra(3)(p14.2) in lymphocytes of lung cancer patients. [electronic resource] by Sundareshan, T S Augustus, M Producer: 19960829 In: Cancer genetics and cytogenetics vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	473.	[The importance of molecular genetic diagnosis of Martin-Bell disease in genetic counseling]. [electronic resource] by Horváth, M Tímár, L Karcagi, V Czeizel, E Producer: 19970415 In: Orvosi hetilap vol. 138 Availability: No items available. Save to lists Add to cart (remove)
	474.	The expression of common fragile sites and genetic predisposition to squamous cell lung cancers. [electronic resource] by Egeli, U Karadağ, M Tunca, B Ozyardímcí, N Producer: 19970618 In: Cancer genetics and cytogenetics vol. 95 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	475.	Low-frequency common fragile sites: link to neuropsychiatric disorders? [electronic resource] by Savelyeva, Larissa Sagulenko, Evgeny Schmitt, Jens Guido Schwab, Manfred Producer: 20060314 In: Cancer letters vol. 232 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	476.	Homozygous condition for a BrdU-requiring fragile site on chromosome 12. [electronic resource] by Voiculescu, I Back, E Schempp, W Producer: 19910408 In: Human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	477.	[Early diagnosis of fragile X mental retardation syndrome]. [electronic resource] by Kan, C C Maaswinkel-Mooij, P D Veenema, H Producer: 19910110 In: Tijdschrift voor kindergeneeskunde vol. 58 Availability: No items available. Save to lists Add to cart (remove)
	478.	Site-specific chromosomal rearrangements induced in human diploid cells by x-irradiation. [electronic resource] by Kano, Y Little, J B Producer: 19860307 In: Cytogenetics and cell genetics vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	479.	Frequency of tri- or multiradial configurations in fragile X identification. [electronic resource] by Jenkins, E C Duncan, C J Krawczun, M S Berns, L M Sanz, M M Brown, W T Producer: 19860404 In: American journal of medical genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	480.	A case of Shwachman syndrome with increased spontaneous chromosome breakage. [electronic resource] by Tada, H Ri, T Yoshida, H Ishimoto, K Kaneko, M Yamashiro, Y Shinohara, T Producer: 19871223 In: Human genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
Next
Last

Refine your search

Availability

Authors

Topics

Languages

Your search returned 1403 results.