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W Wuyts

Showing results (11-20 of 51) with videos related to

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Systematic and Applied Microbiology|July 6, 2000
Organization of the ribosomal operon 165-235 gene spacer region in representatives of Neisseria gonorrhoeaeM Van Looveren, P Vandamme, W Wuyts, et al.
Biochemical Pharmacology|September 1, 1975
Bile acid-binding activity of dodeca-N-methyl neomycin hexamethochloride and dimethylaminopropyl neomycinH Eyssen, P Claes, W Wuyts, et al.
The European Respiratory Journal|April 2, 2011
Three colleagues with sarcoidosis?A Sibille, P Van Bleyenbergh, K Lagrou, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 16, 2002
[From gene to disease; hereditary multiple exostoses]W Wuyts, J V M G Bovée, P C W Hogendoorn
Clinical Genetics|February 3, 2006
Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genesP Verdyck, B Blaumeiser, M Holder-Espinasse, et al.
American Journal of Medical Genetics|May 9, 2001
Burning down DEFECT11W Wuyts, W Van Hul, O Bartsch, et al.
Case Reports in Vascular Medicine|September 1, 2012
Intima sarcoma of the pulmonary artery mimicking takayasu diseaseC Belge, I Renckens, R Van Puijenbroek, et al.
Cytogenetics and Cell Genetics|April 18, 2001
Assignment of the mouse Extl1 gene to the distal part of chromosome 4 by in situ hybridization and radiation hybrid mappingD Mathysen, W Wuyts, P J Bossuyt, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Calcified Tissue International|November 23, 2006
Identification and molecular characterization of a novel splice-site mutation (G1205C) in the SQSTM1 gene causing Paget's disease of bone in an extended American familyG Beyens, W Wuyts, E Cleiren, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Systematic and Applied Microbiology|July 6, 2000
Organization of the ribosomal operon 165-235 gene spacer region in representatives of Neisseria gonorrhoeaeM Van Looveren, P Vandamme, W Wuyts, et al.
Biochemical Pharmacology|September 1, 1975
Bile acid-binding activity of dodeca-N-methyl neomycin hexamethochloride and dimethylaminopropyl neomycinH Eyssen, P Claes, W Wuyts, et al.
The European Respiratory Journal|April 2, 2011
Three colleagues with sarcoidosis?A Sibille, P Van Bleyenbergh, K Lagrou, et al.
Nederlands Tijdschrift Voor Geneeskunde|February 16, 2002
[From gene to disease; hereditary multiple exostoses]W Wuyts, J V M G Bovée, P C W Hogendoorn
Clinical Genetics|February 3, 2006
Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genesP Verdyck, B Blaumeiser, M Holder-Espinasse, et al.
American Journal of Medical Genetics|May 9, 2001
Burning down DEFECT11W Wuyts, W Van Hul, O Bartsch, et al.
Case Reports in Vascular Medicine|September 1, 2012
Intima sarcoma of the pulmonary artery mimicking takayasu diseaseC Belge, I Renckens, R Van Puijenbroek, et al.
Cytogenetics and Cell Genetics|April 18, 2001
Assignment of the mouse Extl1 gene to the distal part of chromosome 4 by in situ hybridization and radiation hybrid mappingD Mathysen, W Wuyts, P J Bossuyt, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Calcified Tissue International|November 23, 2006
Identification and molecular characterization of a novel splice-site mutation (G1205C) in the SQSTM1 gene causing Paget's disease of bone in an extended American familyG Beyens, W Wuyts, E Cleiren, et al.
Pageof 6