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	1.	Juvenile selective vitamin B₁₂ malabsorption: 50 years after its description-10 years of genetic testing. [electronic resource] by Gräsbeck, Ralph Tanner, Stephan M Producer: 20111206 In: Pediatric research vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Vitamin B12 deficiency in a 15-year old boy due to mutations in the intrinsic factor gene, GIF. [electronic resource] by Overgaard, Ulrik M Tanner, Stephan M Birgens, Henrik S Producer: 20100901 In: British journal of haematology vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Molecular cytogenetic characterization of the KG-1 and KG-1a acute myeloid leukemia cell lines by use of spectral karyotyping and fluorescence in situ hybridization. [electronic resource] by Mrózek, Krzysztof Tanner, Stephan M Heinonen, Kristiina Bloomfield, Clara D Producer: 20031204 In: Genes, chromosomes & cancer vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Imerslund-Gräsbeck syndrome in a 15-year-old German girl caused by compound heterozygous mutations in CUBN. [electronic resource] by Hauck, Fabian H Tanner, Stephan M Henker, Jobst Laass, Martin W Producer: 20080909 In: European journal of pediatrics vol. 167 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Acute lymphoblastic leukemia and vitamin B12 deficiency secondary to a gastric intrinsic factor gene mutation. [electronic resource] by Zia, Ayesha Fışgin, Tunç Sokolowski, Catherine Tanner, Stephan M Savaşan, Süreyya Producer: 20121015 In: Pediatric blood & cancer vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Homozygous mutation in the intrinsic factor gene in a child with severe vitamin B12 deficiency]. [electronic resource] by Leunbach, Tina Lund Johansen, Preben Tanner, Stephan M Gräsbeck, Ralph Helgestad, Jon Producer: 20121126 In: Ugeskrift for laeger vol. 173 Availability: No items available. Save to lists Add to cart (remove)
	7.	Investigation of the ABC transporter MRP1 in selected patients with presumed defects in vitamin B12 absorption. [electronic resource] by Shah, Nidhi P Beech, Cameron M Sturm, Amy C Tanner, Stephan M Producer: 20110713 In: Blood vol. 117 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Molecular profiling of chronic lymphocytic leukaemia: genetics meets epigenetics to identify predisposing genes. [electronic resource] by Plass, Christoph Byrd, John C Raval, Aparna Tanner, Stephan M de la Chapelle, Albert Producer: 20080410 In: British journal of haematology vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Baalc, a marker of mesoderm and muscle. [electronic resource] by Satoskar, Anjali A Tanner, Stephan M Weinstein, Michael Qualman, Stephen J de la Chapelle, Albert Producer: 20051115 In: Gene expression patterns : GEP vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Familial peripheral keratopathy without PAX6 mutation. [electronic resource] by Smith, Wendy M Lange, Julie M Sturm, Amy C Tanner, Stephan M Mauger, Thomas F Producer: 20120306 In: Cornea vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Inherited cobalamin malabsorption. Mutations in three genes reveal functional and ethnic patterns. [electronic resource] by Tanner, Stephan M Sturm, Amy C Baack, Elizabeth C Liyanarachchi, Sandya de la Chapelle, Albert Producer: 20130214 In: Orphanet journal of rare diseases vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in Jordan. [electronic resource] by Al-Alami, Jamil R Tanner, Stephan M Tayeh, Marwan K de la Chapelle, Albert El-Shanti, Hatem Producer: 20051103 In: Saudi medical journal vol. 26 Availability: No items available. Save to lists Add to cart (remove)
	13.	Juvenile cobalamin deficiency in a 17-year-old child with autonomic dysfunction and skin changes. [electronic resource] by Siddiqui, Abdul Hafeez Ansari, Aamir Beech, Cameron M Shah, Nidhi P Tanner, Stephan M Sarnaik, Sharada A Producer: 20120409 In: Journal of pediatric hematology/oncology vol. 34 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Imerslund-Grasbeck syndrome associated with recurrent aphthous stomatitis and defective neutrophil function. [electronic resource] by Broides, Arnon Yerushalmi, Baruch Levy, Rachel Hadad, Nurit Kaplun, Norma Tanner, Stephan M Chapelle, Allbert de la Levy, Jacov Producer: 20061219 In: Journal of pediatric hematology/oncology vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Allele-specific expression of TGFBR1 in colon cancer patients. [electronic resource] by Tomsic, Jerneja Guda, Kishore Liyanarachchi, Sandya Hampel, Heather Natale, Leanna Markowitz, Sanford D Tanner, Stephan M de la Chapelle, Albert Producer: 20101110 In: Carcinogenesis vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Ancient founder mutation is responsible for Imerslund-Gräsbeck Syndrome among diverse ethnicities. [electronic resource] by Beech, Cameron M Liyanarachchi, Sandya Shah, Nidhi P Sturm, Amy C Sadiq, May F de la Chapelle, Albert Tanner, Stephan M Producer: 20120229 In: Orphanet journal of rare diseases vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Juvenile cobalamin deficiency in individuals of African ancestry is caused by a founder mutation in the intrinsic factor gene GIF. [electronic resource] by Ament, Andrea E Li, Zhongyuan Sturm, Amy C Perko, James D Lawson, Sarah Masterson, Margaret Quadros, Edward V Tanner, Stephan M Producer: 20090402 In: British journal of haematology vol. 144 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	The functional cobalamin (vitamin B12)-intrinsic factor receptor is a novel complex of cubilin and amnionless. [electronic resource] by Fyfe, John C Madsen, Mette Højrup, Peter Christensen, Erik I Tanner, Stephan M de la Chapelle, Albert He, Qianchuan Moestrup, Søren K Producer: 20040420 In: Blood vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Hereditary intrinsic factor deficiency in chaldeans. [electronic resource] by Sturm, Amy C Baack, Elizabeth C Armstrong, Michael B Schiff, Deborah Zia, Ayesha Savasan, Sureyya de la Chapelle, Albert Tanner, Stephan M Producer: 20130225 In: JIMD reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	BAALC, a novel marker of human hematopoietic progenitor cells. [electronic resource] by Baldus, Claudia D Tanner, Stephan M Kusewitt, Donna F Liyanarachchi, Sandya Choi, Changsun Caligiuri, Michael A Bloomfield, Clara D de la Chapelle, Albert Producer: 20031210 In: Experimental hematology vol. 31 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 37 results.