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Human Mutation|April 23, 2002
Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genesKerstin Kutsche, Bernadette Ressler, Heide-Gertrude Katzera, et al.Proteomics|March 23, 2006
Diagnosis of congenital disorders of glycosylation type-I using protein chip technologyKevin Mills, Philippa Mills, Marie Jackson, et al.Journal of Nephrology|July 14, 2005
Renal failure and hypertension in Alagille syndrome with a novel JAG1 mutationSigrid Harendza, Christian A Hübner, Christiane Gläser, et al.Human Mutation|February 22, 2002
Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1DBenigna von Brederlow, Hanno Bolz, Andreas Janecke, et al.Human Molecular Genetics|January 16, 2007
A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formationFrançois Foulquier, Daniel Ungar, Ellen Reynders, et al.Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology|April 1, 2019
Expression of cornulin in oral premalignant lesionsNeetha Santosh, Kristin K McNamara, F Michael Beck, et al.Klinische Padiatrie|May 3, 2017
[Lysosomal Storage Diseases: Challenges in Multiprofessional Patient Care with Enzyme Replacement Therapy]Anibh Martin Das, Florian Lagler, Michael Beck, et al.Pediatric Dentistry|June 2, 2005
Attitudes of contemporary parents toward behavior management techniques used in pediatric dentistryJonathan J Eaton, Dennis J McTigue, Henry W Fields, et al.Herz|November 20, 2002
Fabry disease: focus on cardiac manifestations and molecular mechanismsAndreas Perrot, Karl Josef Osterziel, Michael Beck, et al.Psychiatrische Praxis|October 31, 2003
[Stigma as perceived by schizophrenics and depressives]Anita Holzinger, Michael Beck, Ingrid Munk, et al.Pageof 31