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	1	SCID Stuttgart : Thieme, Juni 2017
	2	Variant PIK3R1 Hypermorphic Mutation and Clinical Phenotypes in a Family with Short Statures, Mild Immunodeficiency and Lymphoma Enthalten in Klinische Pädiatrie Bd. 229, 2017, Nr. 03: 113-117
	3	Disturbed B-lymphocytes selection in autoimmune lymphoproliferative syndrome Enthalten in Molecular and Cellular Pediatrics Bd. 2, 1.7.2015, Nr. 1, date:12.2015: 1-3
	4	Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy Enthalten in Nature genetics Bd. 50, 26.2.2018, Nr. 3, date:3.2018: 344-348