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H G Brunner

Showing results (81-90 of 179) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1997
Assignment of WNT7B to human chromosome band 22q13 by in situ hybridizationH van Bokhoven, J Kissing, M Schepens, et al.
Clinical Science (London, England : 1979)|May 1, 1995
Plasma metadrenalines: do they provide useful information about sympatho-adrenal function and catecholamine metabolism?G Eisenhofer, P Friberg, K Pacak, et al.
Familial Cancer|February 8, 2012
Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist's initiativeK M Landsbergen, J B Prins, H G Brunner, et al.
Human Reproduction (Oxford, England)|November 6, 1998
Does intracytoplasmic sperm injection lead to a rise in the frequency of microdeletions in the AZFc region of the Y chromosome in future generations?J A Kremer, J H Tuerlings, G Borm, et al.
Molecular Syndromology|July 24, 2012
A 380-kb Duplication in 7p22.3 Encompassing the LFNG Gene in a Boy with Asperger SyndromeA T Vulto-van Silfhout, A F M de Brouwer, N de Leeuw, et al.
Journal of Medical Genetics|August 1, 1994
Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended familyC E de Die-Smulders, C J Höweler, J F Mirandolle, et al.
Neuromuscular Disorders : NMD|December 4, 2001
A new phenotype of autosomal dominant nemaline myopathyI M P Gommans, B G M van Engelen, H J ter Laak, et al.
The Journal of Clinical Investigation|September 1, 1996
Benign familial hematuria due to mutation of the type IV collagen alpha4 geneH H Lemmink, W N Nillesen, T Mochizuki, et al.
Clinical Genetics|January 10, 2003
Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCCN Hoogerbrugge, R Willems, H J Van Krieken, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
Pageof 18

Showing results (81-90 of 179) with videos related to

Sort By:
Pageof 18
Cytogenetics and Cell Genetics|January 1, 1997
Assignment of WNT7B to human chromosome band 22q13 by in situ hybridizationH van Bokhoven, J Kissing, M Schepens, et al.
Clinical Science (London, England : 1979)|May 1, 1995
Plasma metadrenalines: do they provide useful information about sympatho-adrenal function and catecholamine metabolism?G Eisenhofer, P Friberg, K Pacak, et al.
Familial Cancer|February 8, 2012
Psychological distress in newly diagnosed colorectal cancer patients following microsatellite instability testing for Lynch syndrome on the pathologist's initiativeK M Landsbergen, J B Prins, H G Brunner, et al.
Human Reproduction (Oxford, England)|November 6, 1998
Does intracytoplasmic sperm injection lead to a rise in the frequency of microdeletions in the AZFc region of the Y chromosome in future generations?J A Kremer, J H Tuerlings, G Borm, et al.
Molecular Syndromology|July 24, 2012
A 380-kb Duplication in 7p22.3 Encompassing the LFNG Gene in a Boy with Asperger SyndromeA T Vulto-van Silfhout, A F M de Brouwer, N de Leeuw, et al.
Journal of Medical Genetics|August 1, 1994
Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended familyC E de Die-Smulders, C J Höweler, J F Mirandolle, et al.
Neuromuscular Disorders : NMD|December 4, 2001
A new phenotype of autosomal dominant nemaline myopathyI M P Gommans, B G M van Engelen, H J ter Laak, et al.
The Journal of Clinical Investigation|September 1, 1996
Benign familial hematuria due to mutation of the type IV collagen alpha4 geneH H Lemmink, W N Nillesen, T Mochizuki, et al.
Clinical Genetics|January 10, 2003
Very low incidence of microsatellite instability in rectal cancers from families at risk for HNPCCN Hoogerbrugge, R Willems, H J Van Krieken, et al.
Human Genetics|March 1, 1989
Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM)H G Brunner, R G Korneluk, M Coerwinkel-Driessen, et al.
Pageof 18