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	1.	Chromosome aberrations in a large series of spontaneous miscarriages in the German population and review of the literature. [electronic resource] by Jenderny, Jutta Producer: 20140630 In: Molecular cytogenetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Inheritance of a t(13;14)(q10;q10) Robertsonian translocation with a low level of trisomy 13 mosaicism. [electronic resource] by Jenderny, Jutta Schmidt, Winfried Bartsch, Oliver Producer: 20100903 In: European journal of pediatrics vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Chromosome aberrations identified by cytogenetic analysis of the first two clones of cultured amniotic fluid cells compared with QF-PCR results. [electronic resource] by Jenderny, Jutta Schmidt, Winfried Kochhan, Lothar Producer: 20140731 In: Cytogenetic and genome research vol. 142 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Detection of clonal aberrations by cytogenetic analysis after different culture methods and by FISH in 129 patients with Chronic Lymphocytic Leukemia. [electronic resource] by Jenderny, Jutta Goldmann, Claudia Thede, Rebekka Ebrecht, Monika Korioth, Frank Producer: 20150424 In: Cytogenetic and genome research vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mosaic and complete tetraploidy in live-born infants: two new patients and review of the literature. [electronic resource] by Stefanova, Irina Jenderny, Jutta Kaminsky, Elke Mannhardt, Anca Meinecke, Peter Grozdanova, Liliana Gillessen-Kaesbach, Gabriele Producer: 20100901 In: Clinical dysmorphology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	No significantly increased frequency of the inversion polymorphism at the WBS-critical region 7q11.23 in German parents of patients with Williams-Beuren syndrome as compared to a population control. [electronic resource] by Frohnauer, Judith Caliebe, Almuth Gesk, Stefan Partsch, Carl-Joachim Siebert, Reiner Pankau, Rainer Jenderny, Jutta Producer: 20110714 In: Molecular cytogenetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Common variable immunodeficiency, impaired neurological development and reduced numbers of T regulatory cells in a 10-year-old boy with a STAT1 gain-of-function mutation. [electronic resource] by Kobbe, Robin Kolster, Manuela Fuchs, Sebastian Schulze-Sturm, Ulf Jenderny, Jutta Kochhan, Lothar Staab, Julia Tolosa, Eva Grimbacher, Bodo Meyer, Thomas Producer: 20170406 In: Gene vol. 586 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)