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Acta Radiologica: Diagnosis
|
January 1, 1978
Stereotactic computer tomography for biopsy of gliomas
R 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 antigens
H 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 mutation
J Hendrickx, J Wauters, P Coucke, et al.
Human Molecular Genetics
|
April 1, 1993
Fucosidosis: four new mutations and a new polymorphism
H 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 gene
E Fransen, C Schrander-Stumpel, L Vits, et al.
Cancer Research
|
April 1, 1995
Instability of microsatellites in human gliomas
E 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 dismutase
J 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 vivo
W 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 syndrome
K 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-p15
L Van Laer, G Van Camp, E D Green, et al.
Page
of 54
Search research articles
Search
Showing results (231-240 of 531) with videos related to
Sort By:
Page
of 54
Acta Radiologica: Diagnosis
|
January 1, 1978
Stereotactic computer tomography for biopsy of gliomas
R 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 antigens
H 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 mutation
J Hendrickx, J Wauters, P Coucke, et al.
Human Molecular Genetics
|
April 1, 1993
Fucosidosis: four new mutations and a new polymorphism
H 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 gene
E Fransen, C Schrander-Stumpel, L Vits, et al.
Cancer Research
|
April 1, 1995
Instability of microsatellites in human gliomas
E 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 dismutase
J 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 vivo
W 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 syndrome
K 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-p15
L Van Laer, G Van Camp, E D Green, et al.
Page
of 54