Your search returned 92 results.

Results
	81.	Abnormal methylation pattern in constitutive and facultative (X inactive chromosome) heterochromatin of ICF patients. [electronic resource] by Miniou, P Jeanpierre, M Blanquet, V Sibella, V Bonneau, D Herbelin, C Fischer, A Niveleau, A Viegas-Péquignot, E Producer: 19950413 In: Human molecular genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	82.	The prosomal RNA-binding protein p27K is a member of the alpha-type human prosomal gene family. [electronic resource] by Bey, F Silva Pereira, I Coux, O Viegas-Péquignot, E Recillas Targa, F Nothwang, H G Dutrillaux, B Scherrer, K Producer: 19930416 In: Molecular & general genetics : MGG vol. 237 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	83.	The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region. [electronic resource] by Rossignol, S Steunou, V Chalas, C Kerjean, A Rigolet, M Viegas-Pequignot, E Jouannet, P Le Bouc, Y Gicquel, C Producer: 20061211 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	84.	Construction and characterization of a partial library of yeast artificial chromosomes from human chromosome 21. [electronic resource] by Bellis, M Gérard, A Charlieu, J P Marçais, B Brun, M E Viegas-Péquignot, E Carter, D A Roizès, G Producer: 19910620 In: DNA and cell biology vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	85.	Abnormal methylation does not prevent X inactivation in ICF patients. [electronic resource] by Bourc'his, D Miniou, P Jeanpierre, M Molina Gomes, D Dupont, J De Saint-Basile, G Maraschio, P Tiepolo, L Viegas-Péquignot, E Producer: 19990722 In: Cytogenetics and cell genetics vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	86.	Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3. [electronic resource] by Delattre, O Bernard, A Malfoy, B Marlhens, F Viegas-Pequignot, E Brossard, C Haguenauer, O Creau-Goldberg, N Van Cong, N Dutrillaux, B Producer: 19871217 In: Nucleic acids research vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	87.	Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe. [electronic resource] by Delattre, O Bernard, A Malfoy, B Marlhens, F Viegas-Pequignot, E Brossard, C Haguenauer, O Creau-Goldberg, N N'guyen, V C Dutrillaux, B Producer: 19880826 In: Human heredity vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	88.	Whole-genome methylation scan in ICF syndrome: hypomethylation of non-satellite DNA repeats D4Z4 and NBL2. [electronic resource] by Kondo, T Bobek, M P Kuick, R Lamb, B Zhu, X Narayan, A Bourc'his, D Viegas-Péquignot, E Ehrlich, M Hanash, S M Producer: 20000414 In: Human molecular genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	89.	The gene for the ligand binding chain of the human interferon gamma receptor. [electronic resource] by Merlin, G van der Leede, B J McKune, K Knezevic, N Bannwarth, W Romquin, N Viegas-Pequignot, E Kiefer, H Aguet, M Dembic, Z Producer: 19970522 In: Immunogenetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	90.	Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene. [electronic resource] by Xu, G L Bestor, T H Bourc'his, D Hsieh, C L Tommerup, N Bugge, M Hulten, M Qu, X Russo, J J Viegas-Péquignot, E Producer: 20000203 In: Nature vol. 402 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	91.	Structure and physical mapping of DR1, a TATA-binding protein-associated phosphoprotein gene, to chromosome 1p22.1 and its exclusion in Stargardt disease (STGD). [electronic resource] by Rozet, J M Gerber, S Perrault, I Camuzat, A Calvas, P Viegas-Pequignot, E Molina-Gomes, D Le Paslier, D Chumakov, I Munnich, A Kaplan, J Producer: 19970211 In: Genomics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	92.	DNMT3B mutations and DNA methylation defect define two types of ICF syndrome. [electronic resource] by Jiang, Y L Rigolet, M Bourc'his, D Nigon, F Bokesoy, I Fryns, J P Hultén, M Jonveaux, P Maraschio, P Mégarbané, A Moncla, A Viegas-Péquignot, E Producer: 20060227 In: Human mutation vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

First
Previous
1
2
3
4
5