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	1.	Identification of Novel Susceptibility Genes for Breast Cancer - Genome-Wide Association Studies or Evaluation of Candidate Genes? [electronic resource] by Meindl, Alfons Publication details: Breast care (Basel, Switzerland) In: Breast care (Basel, Switzerland) vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Breast cancer susceptibility: current knowledge and implications for genetic counselling. [electronic resource] by Ripperger, Tim Gadzicki, Dorothea Meindl, Alfons Schlegelberger, Brigitte Producer: 20090901 In: European journal of human genetics : EJHG vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Hereditary breast and ovarian cancer: new genes, new treatments, new concepts. [electronic resource] by Meindl, Alfons Ditsch, Nina Kast, Karin Rhiem, Kerstin Schmutzler, Rita K Producer: 20120319 In: Deutsches Arzteblatt international vol. 108 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Vitamin D receptor, Retinoid X receptor and peroxisome proliferator-activated receptor γ are overexpressed in BRCA1 mutated breast cancer and predict prognosis. [electronic resource] by Heublein, Sabine Mayr, Doris Meindl, Alfons Kircher, Alexandra Jeschke, Udo Ditsch, Nina Producer: 20180205 In: Journal of experimental & clinical cancer research : CR vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative disease. [electronic resource] by Hügle, Boris Astigarraga, Itziar Henter, Jan-Inge Porwit-MacDonald, Anna Meindl, Alfons Schuster, Volker Producer: 20070920 In: European journal of pediatrics vol. 166 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	The genotype of the original Wiskott phenotype. [electronic resource] by Binder, Vera Albert, Michael H Kabus, Maria Bertone, Marko Meindl, Alfons Belohradsky, Bernd H Producer: 20061101 In: The New England journal of medicine vol. 355 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A novel mutation in the interleukin-2 receptor gamma gene as the cause of lymphopenia in a neonate vertically exposed to human immunodeficiency virus. [electronic resource] by Neubert, Jennifer Meindl, Alfons Theisen, Albert Adams, Ortwin Schulz, Ansgar Feyen, Oliver Niehues, Tim Producer: 20050516 In: The Pediatric infectious disease journal vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Two new families with X-linked inhibitor of apoptosis deficiency and a review of all 26 published cases. [electronic resource] by Horn, Peter C Belohradsky, Bernd H Urban, Christian Weber-Mzell, Daniela Meindl, Alfons Schuster, Volker Producer: 20110318 In: The Journal of allergy and clinical immunology vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	KIF21A variant R954W in familial or sporadic cases of CFEOM1. [electronic resource] by Rudolph, Guenther Nentwich, Michael Hellebrand, Heide Pollack, Katharina Gordes, Roswitha Bau, Viktoria Kampik, Anselm Meindl, Alfons Producer: 20091124 In: European journal of ophthalmology vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22. [electronic resource] by Golla, Astrid Jansson, Annette Ramser, Juliane Hellebrand, Heide Zahn, Robert Meitinger, Thomas Belohradsky, Bernd H Meindl, Alfons Producer: 20020812 In: European journal of human genetics : EJHG vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Phenotypic expression of the complete type of X-linked congenital stationary night blindness in patients with different mutations in the NYX gene. [electronic resource] by Jacobi, Felix K Andréasson, Sten Langrova, Hana Meindl, Alfons Zrenner, Eberhart Apfelstedt-Sylla, Eckart Pusch, Carsten M Producer: 20030204 In: Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie vol. 240 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Validation of mRNA/EST-based gene predictions in human Xp11.4 revealed differences to the organization of the orthologous mouse locus. [electronic resource] by Wen, Gaiping Ramser, Juliane Taudien, Stefan Gausmann, Ulrike Blechschmidt, Karin Frankish, Adam Ashurst, Jennifer Meindl, Alfons Platzer, Matthias Producer: 20060203 In: Mammalian genome : official journal of the International Mammalian Genome Society vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Strong association of a common dihydropyrimidine dehydrogenase gene polymorphism with fluoropyrimidine-related toxicity in cancer patients. [electronic resource] by Gross, Eva Busse, Birgit Riemenschneider, Matthias Neubauer, Steffi Seck, Katharina Klein, Hanns-Georg Kiechle, Marion Lordick, Florian Meindl, Alfons Producer: 20090213 In: PloS one vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Detailed analysis of five mutations in dihydropyrimidine dehydrogenase detected in cancer patients with 5-fluorouracil-related side effects. [electronic resource] by Gross, Eva Ullrich, Tobias Seck, Katharina Mueller, Volkmar de Wit, Maike von Schilling, Christoph Meindl, Alfons Schmitt, Manfred Kiechle, Marion Producer: 20040126 In: Human mutation vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation. [electronic resource] by Martínez-Garay, Isabel Tomás, Miguel Oltra, Silvestre Ramser, Juliane Moltó, Maria D Prieto, Félix Meindl, Alfons Kutsche, Kerstin Martínez, Francisco Producer: 20070329 In: European journal of human genetics : EJHG vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Refinement of the physical location and the genomic characterization of the CRSP2 (EXLM1) gene on Xp11.4. [electronic resource] by Demirci, F Yesim Ramser, Juliane White, Nicola J Rigatti, Brian W Meindl, Alfons Lewis, Karen F Wen, Gaiping Gorin, Michael B Producer: 20040115 In: DNA sequence : the journal of DNA sequencing and mapping vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	A mild phenotype of dihydropyrimidine dehydrogenase deficiency and developmental retardation associated with a missense mutation affecting cofactor binding. [electronic resource] by Weidensee, Sabine Goettig, Peter Bertone, Marko Haas, Dorothea Magdolen, Viktor Kiechle, Marion Meindl, Alfons van Kuilenburg, André B P Gross, Eva Producer: 20111004 In: Clinical biochemistry vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Allelic loss analysis by denaturing high-performance liquid chromatography and electrospray ionization mass spectrometry. [electronic resource] by Gross, Eva Hölzl, Georg Arnold, Norbert Hauenstein, Evelyn Jacobsen, Anja Schulze, Kathrin Ramser, Juliane Meindl, Alfons Kiechle, Marion Oefner, Peter J Producer: 20070316 In: Human mutation vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Variable number of tandem repeats polymorphism in the SMYD3 promoter region and the risk of familial breast cancer. [electronic resource] by Frank, Bernd Hemminki, Kari Wappenschmidt, Barbara Klaes, Rüdiger Meindl, Alfons Schmutzler, Rita K Bugert, Peter Untch, Michael Bartram, Claus R Burwinkel, Barbara Producer: 20060522 In: International journal of cancer vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	BRIP1 (BACH1) variants and familial breast cancer risk: a case-control study. [electronic resource] by Frank, Bernd Hemminki, Kari Meindl, Alfons Wappenschmidt, Barbara Sutter, Christian Kiechle, Marion Bugert, Peter Schmutzler, Rita K Bartram, Claus R Burwinkel, Barbara Producer: 20070709 In: BMC cancer vol. 7 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 222 results.