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Han G Brunner

Showing results (21-30 of 318) with videos related to

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American Journal of Medical Genetics|October 3, 2002
P63 gene mutations and human developmental syndromesHan G Brunner, Ben C J Hamel, Hans van Bokhoven Hv
BMC Bioinformatics|April 25, 2008
Conserved co-expression for candidate disease gene prioritizationMartin Oti, Jeroen van Reeuwijk, Martijn A Huynen, et al.
Nature Human Behaviour|May 15, 2025
Reproductive and cognitive phenotypes in carriers of recessive pathogenic variantsHila Fridman, Gelana Khazeeva, Ephrat Levy-Lahad, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2002
The relationship between clinical severity of Noonan's syndrome and growth, growth hormone (GH) secretion and response to GH treatmentKees Noordam, Ineke van der Burgt, Han G Brunner, et al.
BMC Bioinformatics|December 6, 2013
Status quo of annotation of human disease variantsHanka Venselaar, Franscesca Camilli, Shima Gholizadeh, et al.
Familial Cancer|March 31, 2009
Genetic testing for Lynch syndrome in the first year of colorectal cancer: a review of the psychological impactKarin M Landsbergen, Judith B Prins, Han G Brunner, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|March 16, 2023
Autism spectrum disorder and brain volume link through a set of mTOR-related genesMartina Arenella, Nina R Mota, Mariel W A Teunissen, et al.
International Journal of Molecular Sciences|July 14, 2023
An E280K Missense Variant in <i>KCND3</i>/Kv4.3-Case Report and Functional CharacterizationRichard Ågren, Niels Geerdink, Han G Brunner, et al.
Familial Cancer|December 8, 2009
Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 yearsKarin M Landsbergen, Judith B Prins, Yvonne J L Kamm, et al.
Human Molecular Genetics|October 26, 2005
Identification of disease genes by whole genome CGH arraysLisenka E L M Vissers, Joris A Veltman, Ad Geurts van Kessel, et al.
Pageof 32

Showing results (21-30 of 318) with videos related to

Sort By:
Pageof 32
American Journal of Medical Genetics|October 3, 2002
P63 gene mutations and human developmental syndromesHan G Brunner, Ben C J Hamel, Hans van Bokhoven Hv
BMC Bioinformatics|April 25, 2008
Conserved co-expression for candidate disease gene prioritizationMartin Oti, Jeroen van Reeuwijk, Martijn A Huynen, et al.
Nature Human Behaviour|May 15, 2025
Reproductive and cognitive phenotypes in carriers of recessive pathogenic variantsHila Fridman, Gelana Khazeeva, Ephrat Levy-Lahad, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 5, 2002
The relationship between clinical severity of Noonan's syndrome and growth, growth hormone (GH) secretion and response to GH treatmentKees Noordam, Ineke van der Burgt, Han G Brunner, et al.
BMC Bioinformatics|December 6, 2013
Status quo of annotation of human disease variantsHanka Venselaar, Franscesca Camilli, Shima Gholizadeh, et al.
Familial Cancer|March 31, 2009
Genetic testing for Lynch syndrome in the first year of colorectal cancer: a review of the psychological impactKarin M Landsbergen, Judith B Prins, Han G Brunner, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|March 16, 2023
Autism spectrum disorder and brain volume link through a set of mTOR-related genesMartina Arenella, Nina R Mota, Mariel W A Teunissen, et al.
International Journal of Molecular Sciences|July 14, 2023
An E280K Missense Variant in <i>KCND3</i>/Kv4.3-Case Report and Functional CharacterizationRichard Ågren, Niels Geerdink, Han G Brunner, et al.
Familial Cancer|December 8, 2009
Female BRCA mutation carriers with a preference for prophylactic mastectomy are more likely to participate an educational-support group and to proceed with the preferred intervention within 2 yearsKarin M Landsbergen, Judith B Prins, Yvonne J L Kamm, et al.
Human Molecular Genetics|October 26, 2005
Identification of disease genes by whole genome CGH arraysLisenka E L M Vissers, Joris A Veltman, Ad Geurts van Kessel, et al.
Pageof 32