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	21.	Increased angiogenesis in portal hypertensive rats: role of nitric oxide. [electronic resource] by Sumanovski, L T Battegay, E Stumm, M van der Kooij, M Sieber, C C Producer: 19990520 In: Hepatology (Baltimore, Md.) vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Partial trisomy 9p12p21.3 with a normal phenotype. [electronic resource] by Stumm, M Müsebeck, J Tönnies, H Volleth, M Lemke, J Chudoba, I Wieacker, P Producer: 20020305 In: Journal of medical genetics vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Female pseudohermaphroditism caused by caudal dysgenesis. [electronic resource] by Wieacker, P Grumpelt, U Schulz, T Gharavi, B Avenarius, S Jakubiczka, S Stumm, M Producer: 20010329 In: Cytogenetics and cell genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Molecular characterization of the DICE1 (DDX26) tumor suppressor gene in lung carcinoma cells. [electronic resource] by Wieland, I Röpke, A Stumm, M Sell, C Weidle, U H Wieacker, P F Producer: 20020913 In: Oncology research vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	In vivo angiogenesis in normal and portal hypertensive rats: role of basic fibroblast growth factor and nitric oxide. [electronic resource] by Sieber, C C Sumanovski, L T Stumm, M van der Kooij, M Battegay, E Producer: 20011205 In: Journal of hepatology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	No evidence for deletions of the NBS1 gene in lymphomas. [electronic resource] by Stumm, M von Ruskowsky, A Siebert, R Harder, S Varon, R Wieacker, P Schlegelberger, B Producer: 20010614 In: Cancer genetics and cytogenetics vol. 126 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Familial occurrence of a del(Xp-) chromosome: pitfall in karyotype/phenotype correlation. [electronic resource] by Soyke, A Stumm, M Krebs, P Kloos, D U Wieacker, P Mohnike, K Elsner, J Producer: 19990217 In: American journal of medical genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	First-trimester prenatal diagnosis of Okihiro syndrome. [electronic resource] by Becker, R Horn, D Knoll, U Stumm, M Wegner, R D Peters, H Sarioglu, N Producer: 20101202 In: Fetal diagnosis and therapy vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	[Structure and chromosomal localization of human neurogranin gene]. [electronic resource] by Mertsalov, I B Stumm, M Wieacker, P tom Dieck, S Gundelfinger, E Tsetlin, V I Producer: 19980306 In: Bioorganicheskaia khimiia vol. 23 Availability: No items available. Save to lists Add to cart (remove)
	30.	Two further cases of WHS with unbalanced de novo translocation t(4;8) characterised by CGH and FISH. [electronic resource] by Tönnies, H Stumm, M Neumann, L Volleth, M Grumpelt, U Müsebeck, J Annuss, G Neitzel, H Producer: 20011011 In: Journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	The differential expression of proinflammatory cytokines IL-6, IL-8 and TNF-alpha in renal cell carcinoma. [electronic resource] by König, B Steinbach, F Janocha, B Drynda, A Stumm, M Philipp, C Allhoff, E P König, W Producer: 19990629 In: Anticancer research vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	32.	Improved definition of chromosomal breakpoints using high-resolution multicolour banding. [electronic resource] by Lemke, J Chudoba, I Senger, G Stumm, M Loncarevic, I F Henry, C Zabel, B Claussen, U Producer: 20010823 In: Human genetics vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCR. [electronic resource] by Stumm, M Boger, E Gaissmaier, C G Oßwald, C Blankenburg, M Wegner, R D Mollenhauer, J A Producer: 20121227 In: Osteoarthritis and cartilage vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal age. [electronic resource] by Hagen, A Entezami, M Gasiorek-Wiens, A Albig, M Becker, R Knoll, U Stumm, M Wegner, R-D Producer: 20111205 In: Ultraschall in der Medizin (Stuttgart, Germany : 1980) vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	Frequency of CFTR gene mutations in males participating in an ICSI programme. [electronic resource] by Jakubiczka, S Bettecken, T Stumm, M Nickel, I Müsebeck, J Krebs, P Fischer, C Kleinstein, J Wieacker, P Producer: 19990913 In: Human reproduction (Oxford, England) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1. [electronic resource] by Stumm, M Gatti, R A Reis, A Udar, N Chrzanowska, K Seemanova, E Sperling, K Wegner, R D Producer: 19951103 In: American journal of human genetics vol. 57 Availability: No items available. Save to lists Add to cart (remove)
	37.	FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy. [electronic resource] by Bartsch, O Wagner, A Hinkel, G K Krebs, P Stumm, M Schmalenberger, B Böhm, S Balci, S Majewski, F Producer: 20000120 In: European journal of human genetics : EJHG vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short stature. [electronic resource] by Musebeck, J Mohnike, K Beye, P Tönnies, H Neitzel, H Schnabel, D Grüters, A Wieacker, P F Stumm, M Producer: 20020301 In: European journal of pediatrics vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing. [electronic resource] by Jakubiczka, S Mitulla, B Liehr, T Arnemann, J Lehrach, H Sudbrak, R Stumm, M Wieacker, P F Bettecken, T Producer: 20001228 In: Prenatal diagnosis vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence. [electronic resource] by Stanulla, M Stümm, M Dieckvoss, B O Seidemann, K Schemmel, V Müller Brechlin, A Schrappe, M Welte, K Reiter, A Producer: 20000712 In: British journal of haematology vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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