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	101.	Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy. [electronic resource] by Schinzel, A Kotzot, D Brecevic, L Robinson, W P Dutly, F Dauwerse, H Binkert, F Baumer, A Ausserer, B Producer: 19980121 In: European journal of human genetics : EJHG vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	102.	M-FISH applications in clinical genetics. [electronic resource] by Cetin, Z Berker Karaüzüm, S Yakut, S Mihçi, E Baumer, A Wey, E Taçoy, S Bağci, G Lüleci, G Producer: 20060215 In: Genetic counseling (Geneva, Switzerland) vol. 16 Availability: No items available. Save to lists Add to cart (remove)
	103.	Endothelial dysfunction and oxidative stress during estrogen deficiency in spontaneously hypertensive rats. [electronic resource] by Wassmann, S Bäumer, A T Strehlow, K van Eickels , M Grohé, C Ahlbory, K Rösen, R Böhm, M Nickenig, G Producer: 20010426 In: Circulation vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	104.	Mitochondrial DNA mutation associated with aging and degenerative disease. [electronic resource] by Nagley, P Mackay, I R Baumer, A Maxwell, R J Vaillant, F Wang, Z X Zhang, C Linnane, A W Producer: 19930217 In: Annals of the New York Academy of Sciences vol. 673 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	105.	Variants in neurotrophic factor genes and schizophrenic psychoses: no associations in a Spanish population. [electronic resource] by Thome, J Durany, N Palomo, A Foley, P Harsányi, A Baumer, A Hashimoto, E Cruz-Sánchez, F F Riederer, P Producer: 19970923 In: Psychiatry research vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	106.	Strong temperature dependence of irradiation effects in organic layers. [electronic resource] by Feulner, P Niedermayer, T Eberle, K Schneider, R Menzel, D Baumer, A Schmich, E Shaporenko, A Tai, Y Zharnikov, M Producer: 20041209 In: Physical review letters vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	107.	A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma. [electronic resource] by Minder, E I Schneider-Yin, X Mamet, R Horev, L Neuenschwander, S Baumer, A Austerlitz, F Puy, H Schoenfeld, N Producer: 20110217 In: Journal of the European Academy of Dermatology and Venereology : JEADV vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	108.	HMG-CoA reductase inhibitors improve endothelial dysfunction in normocholesterolemic hypertension via reduced production of reactive oxygen species. [electronic resource] by Wassmann, S Laufs, U Bäumer, A T Müller, K Ahlbory, K Linz, W Itter, G Rösen, R Böhm, M Nickenig, G Producer: 20010802 In: Hypertension (Dallas, Tex. : 1979) vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	109.	A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindred. [electronic resource] by Häfner, F M Salam, A A Linder, T E Balmer, D Baumer, A Schinzel, A A Spillmann, T Leal, S M Producer: 20000531 In: American journal of human genetics vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	110.	Clinical and genetic heterogeneity in Meckel syndrome. [electronic resource] by Paavola, P Salonen, R Baumer, A Schinzel, A Boyd, P A Gould, S Meusburger, H Tenconi, R Barnicoat, A Winter, R Peltonen, L Producer: 19971224 In: Human genetics vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	111.	Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes. [electronic resource] by Bartholdi, D Krajewska-Walasek, M Ounap, K Gaspar, H Chrzanowska, K H Ilyana, H Kayserili, H Lurie, I W Schinzel, A Baumer, A Producer: 20090521 In: Journal of medical genetics vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	112.	Jacobsen syndrome and Beckwith-Wiedemann syndrome caused by a parental pericentric inversion inv(11)(p15q24). [electronic resource] by Gadzicki, D Baumer, A Wey, E Happel, C M Rudolph, C Tönnies, H Neitzel, H Steinemann, D Welte, K Klein, C Schlegelberger, B Producer: 20061211 In: Annals of human genetics vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	113.	A null mutation allele in the CNTF gene and schizophrenic psychoses. [electronic resource] by Thome, J Durany, N Harsányi, A Foley, P Palomo, A Kornhuber, J Weijers, H G Baumer, A Rösler, M Cruz-Sánchez, F F Beckmann, H Riederer, P Producer: 19970107 In: Neuroreport vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	114.	Estrogen modulates AT1 receptor gene expression in vitro and in vivo. [electronic resource] by Nickenig, G Bäumer, A T Grohè, C Kahlert, S Strehlow, K Rosenkranz, S Stäblein, A Beckers, F Smits, J F Daemen, M J Vetter, H Böhm, M Producer: 19980709 In: Circulation vol. 97 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	115.	Maternal uniparental disomy 7--review and further delineation of the phenotype. [electronic resource] by Kotzot, D Balmer, D Baumer, A Chrzanowska, K Hamel, B C Ilyina, H Krajewska-Walasek, M Lurie, I W Otten, B J Schoenle, E Tariverdian, G Schinzel, A Producer: 20000518 In: European journal of pediatrics vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	116.	Duplications in addition to terminal deletions are present in a proportion of ring chromosomes: clues to the mechanisms of formation. [electronic resource] by Rossi, E Riegel, M Messa, J Gimelli, S Maraschio, P Ciccone, R Stroppi, M Riva, P Perrotta, C S Mattina, T Memo, L Baumer, A Kucinskas, V Castellan, C Schinzel, A Zuffardi, O Producer: 20080403 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	117.	Analysis of quality and feasibility of an objective structured clinical examination (OSCE) in preclinical dental education. [electronic resource] by Eberhard, L Hassel, A Bäumer, A Becker, F Beck-Mubotter, J Bömicke, W Corcodel, N Cosgarea, R Eiffler, C Giannakopoulos, N N Kraus, T Mahabadi, J Rues, S Schmitter, M Wolff, D Wege, K C Producer: 20111121 In: European journal of dental education : official journal of the Association for Dental Education in Europe vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	118.	Characterization of ATM gene mutations in 66 ataxia telangiectasia families. [electronic resource] by Sandoval, N Platzer, M Rosenthal, A Dörk, T Bendix, R Skawran, B Stuhrmann, M Wegner, R D Sperling, K Banin, S Shiloh, Y Baumer, A Bernthaler, U Sennefelder, H Brohm, M Weber, B H Schindler, D Producer: 19990318 In: Human molecular genetics vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	119.	Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications. [electronic resource] by Kotzot, D Martinez, M J Bagci, G Basaran, S Baumer, A Binkert, F Brecevic, L Castellan, C Chrzanowska, K Dutly, F Gutkowska, A Karaüzüm, S B Krajewska-Walasek, M Luleci, G Miny, P Riegel, M Schuffenhauer, S Seidel, H Schinzel, A Producer: 20000516 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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