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J Willems

Showing results (231-240 of 531) with videos related to

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Acta Radiologica: Diagnosis|January 1, 1978
Stereotactic computer tomography for biopsy of gliomasR Lewander, M Bergström, J Boëthius, et al.
Clinical Biochemistry|June 26, 1999
A comparison of ELISA assays as routine diagnostic test for detection of autoantibodies against extractable nuclear antigensH L Van Duijnhoven, F J Van De Warenburg, R J Willems, et al.
Acta Clinica Belgica|January 1, 1991
DNA diagnosis of cystic fibrosis by direct detection of the delta F508 mutationJ Hendrickx, J Wauters, P Coucke, et al.
Human Molecular Genetics|April 1, 1993
Fucosidosis: four new mutations and a new polymorphismH C Seo, P J Willems, K A Kretz, et al.
Human Molecular Genetics|December 1, 1994
X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM geneE Fransen, C Schrander-Stumpel, L Vits, et al.
Cancer Research|April 1, 1995
Instability of microsatellites in human gliomasE Dams, E J Van de Kelft, J J Martin, et al.
FEBS Letters|April 24, 1995
Cadherin-dependent cell aggregation is affected by decapeptide derived from rat extracellular super-oxide dismutaseJ Willems, E Bruyneel, V Noë, et al.
The American Journal of Physiology|September 1, 1982
Sympathetic supraspinal control of venous membrane potential in spontaneous hypertension in vivoW J Willems, D R Harder, S J Contney, et al.
Human Genetics|March 7, 1998
Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndromeK Storm, I Handig, E Reyniers, et al.
Human Genetics|June 1, 1997
Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15L Van Laer, G Van Camp, E D Green, et al.
Pageof 54

Showing results (231-240 of 531) with videos related to

Sort By:
Pageof 54
Acta Radiologica: Diagnosis|January 1, 1978
Stereotactic computer tomography for biopsy of gliomasR Lewander, M Bergström, J Boëthius, et al.
Clinical Biochemistry|June 26, 1999
A comparison of ELISA assays as routine diagnostic test for detection of autoantibodies against extractable nuclear antigensH L Van Duijnhoven, F J Van De Warenburg, R J Willems, et al.
Acta Clinica Belgica|January 1, 1991
DNA diagnosis of cystic fibrosis by direct detection of the delta F508 mutationJ Hendrickx, J Wauters, P Coucke, et al.
Human Molecular Genetics|April 1, 1993
Fucosidosis: four new mutations and a new polymorphismH C Seo, P J Willems, K A Kretz, et al.
Human Molecular Genetics|December 1, 1994
X-linked hydrocephalus and MASA syndrome present in one family are due to a single missense mutation in exon 28 of the L1CAM geneE Fransen, C Schrander-Stumpel, L Vits, et al.
Cancer Research|April 1, 1995
Instability of microsatellites in human gliomasE Dams, E J Van de Kelft, J J Martin, et al.
FEBS Letters|April 24, 1995
Cadherin-dependent cell aggregation is affected by decapeptide derived from rat extracellular super-oxide dismutaseJ Willems, E Bruyneel, V Noë, et al.
The American Journal of Physiology|September 1, 1982
Sympathetic supraspinal control of venous membrane potential in spontaneous hypertension in vivoW J Willems, D R Harder, S J Contney, et al.
Human Genetics|March 7, 1998
Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndromeK Storm, I Handig, E Reyniers, et al.
Human Genetics|June 1, 1997
Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15L Van Laer, G Van Camp, E D Green, et al.
Pageof 54