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	1.	Somatic FGFR3 and PIK3CA mutations are present in familial seborrhoeic keratoses. [electronic resource] by Hafner, C Vogt, T Landthaler, M Müsebeck, J Producer: 20081023 In: The British journal of dermatology vol. 159 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Molecular mechanisms underlying hemophilia A phenotype in seven females. [electronic resource] by Pavlova, A Brondke, H Müsebeck, J Pollmann, H Srivastava, A Oldenburg, J Producer: 20090915 In: Journal of thrombosis and haemostasis : JTH vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	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)
	4.	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)
	5.	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)
	6.	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)
	7.	Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism. [electronic resource] by Liehr, T Ziegler, M Starke, H Heller, A Kuechler, A Kittner, G Beensen, V Seidel, J Hässler, H Müsebeck, J Claussen, U Producer: 20040316 In: Clinical genetics vol. 64 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function. [electronic resource] by Lacbawan, F Solomon, B D Roessler, E El-Jaick, K Domené, S Vélez, J I Zhou, N Hadley, D Balog, J Z Long, R Fryer, A Smith, W Omar, S McLean, S D Clarkson, K Lichty, A Clegg, N J Delgado, M R Levey, E Stashinko, E Potocki, L Vanallen, M I Clayton-Smith, J Donnai, D Bianchi, D W Juliusson, P B Njølstad, P R Brunner, H G Carey, J C Hehr, U Müsebeck, J Wieacker, P F Postra, A Hennekam, R C M van den Boogaard, M-J H van Haeringen, A Paulussen, A Herbergs, J Schrander-Stumpel, C T R M Janecke, A R Chitayat, D Hahn, J McDonald-McGinn, D M Zackai, E H Dobyns, W B Muenke, M Producer: 20090804 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)