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	1.	AlphaPIX and betaPIX and their role in focal adhesion formation. [electronic resource] by Rosenberger, Georg Kutsche, Kerstin Producer: 20060822 In: European journal of cell biology vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Response to Calgani et al. [electronic resource] by Zenker, Martin Kutsche, Kerstin Producer: 20180305 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Interpretation of sequence variants of the FBN1 gene: analog or digital? A commentary on decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants. [electronic resource] by von Kodolitsch, Yskert Kutsche, Kerstin Producer: 20160412 In: Journal of human genetics vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Oncogenic HRAS mutations cause prolonged PI3K signaling in response to epidermal growth factor in fibroblasts of patients with Costello syndrome. [electronic resource] by Rosenberger, Georg Meien, Stefanie Kutsche, Kerstin Producer: 20090528 In: Human mutation vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	AlphaPIX associates with calpain 4, the small subunit of calpain, and has a dual role in integrin-mediated cell spreading. [electronic resource] by Rosenberger, Georg Gal, Andreas Kutsche, Kerstin Producer: 20050408 In: The Journal of biological chemistry vol. 280 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations? [electronic resource] by Wimplinger, Isabella Shaw, Gary M Kutsche, Kerstin Producer: 20071023 In: Molecular vision vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	7.	Interaction of alphaPIX (ARHGEF6) with beta-parvin (PARVB) suggests an involvement of alphaPIX in integrin-mediated signaling. [electronic resource] by Rosenberger, Georg Jantke, Inka Gal, Andreas Kutsche, Kerstin Producer: 20030801 In: Human molecular genetics vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Fragmented Elastic Fibers in Focal Dermal Hypoplasia (Goltz-Gorlin Syndrome) Without Focal Dermal Hypoplasia: Report of a Male Case and Review of the Literature. [electronic resource] by Rohdenburg, Christina Liersch, Julia Kutsche, Kerstin Schaller, Joerg Producer: 20210705 In: The American Journal of dermatopathology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Pontocerebellar hypoplasia type 2 and TSEN2: review of the literature and two novel mutations. [electronic resource] by Bierhals, Tatjana Korenke, Georg Christoph Uyanik, Gökhan Kutsche, Kerstin Producer: 20131104 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Large intragenic deletions of the NF2 gene: breakpoints and associated phenotypes. [electronic resource] by Abo-Dalo, Benjamin Kutsche, Kerstin Mautner, Victor Kluwe, Lan Producer: 20100224 In: Genes, chromosomes & cancer vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Expanding the phenotype associated with 17q12 duplication: case report and review of the literature. [electronic resource] by Bierhals, Tatjana Maddukuri, Satish Babu Kutsche, Kerstin Girisha, Katta Mohan Producer: 20130701 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Zimmermann-Laband syndrome associated with a balanced reciprocal translocation t(3;8)(p21.2;q24.3) in mother and daughter: molecular cytogenetic characterization of the breakpoint regions. [electronic resource] by Stefanova, Margarita Atanassov, Dimitar Krastev, Tzaniu Fuchs, Sigrid Kutsche, Kerstin Producer: 20030807 In: American journal of medical genetics. Part A vol. 117A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody. [electronic resource] by Martinez-Garay, Isabel Rustom, Amin Gerdes, Hans-Hermann Kutsche, Kerstin Producer: 20060703 In: Genomics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Autosomal dominant Robinow syndrome associated with a novel DVL3 splice mutation. [electronic resource] by Danyel, Magdalena Kortüm, Fanny Dathe, Katarina Kutsche, Kerstin Horn, Denise Producer: 20190228 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	de novo MEPCE nonsense variant associated with a neurodevelopmental disorder causes disintegration of 7SK snRNP and enhanced RNA polymerase II activation. [electronic resource] by Schneeberger, Pauline E Bierhals, Tatjana Neu, Axel Hempel, Maja Kutsche, Kerstin Producer: 20201028 In: Scientific reports vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Costello syndrome with severe cutis laxa and mosaic HRAS G12S mutation. [electronic resource] by Girisha, Katta M Lewis, Leslie E Phadke, Shubha R Kutsche, Kerstin Producer: 20110204 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome. [electronic resource] by Wimplinger, Isabella Rauch, Anita Orth, Ulrike Schwarzer, Ulrich Trautmann, Udo Kutsche, Kerstin Producer: 20080311 In: European journal of medical genetics vol. 50 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	A severe form of the X-linked microphthalmia with linear skin defects syndrome in a female newborn. [electronic resource] by Steichen-Gersdorf, Elisabeth Griesmaier, Elke Pientka, Friederike K Kotzot, Dieter Kutsche, Kerstin Producer: 20100526 In: Clinical dysmorphology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Two cases with severe lethal course of Costello syndrome associated with HRAS p.G12C and p.G12D. [electronic resource] by Lorenz, Sybille Petersen, Christine Kordaß, Ulrike Seidel, Heide Zenker, Martin Kutsche, Kerstin Producer: 20130218 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Goltz-Gorlin Syndrome: Revisiting the Clinical Spectrum. [electronic resource] by Yesodharan, Dhanya Büschenfelde, Uta Meyer Zum Kutsche, Kerstin Mohandas Nair, K Nampoothiri, Sheela Producer: 20190111 In: Indian journal of pediatrics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 95 results.