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Showing results (241-250 of 391) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Construction of a map of chromosome 16 by using radiation hybridsI Ceccherini, G Romeo, S Lawrence, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTSJohannes G Dauwerse, Martine van Belzen, Arie van Haeringen, et al.
American Journal of Human Genetics|August 16, 2006
Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferaseSaskia A J Lesnik Oberstein, Marjolein Kriek, Stefan J White, et al.
British Journal of Cancer|May 29, 2003
Genetic counselling and the intention to undergo prophylactic mastectomy: effects of a breast cancer risk assessmentS van Dijk, W Otten, M W Zoeteweij, et al.
Journal of Dental Research|July 26, 2017
Orthodontics with Customized versus Noncustomized Appliances: A Randomized Controlled Clinical TrialE W Penning, R H J Peerlings, J D M Govers, et al.
Genomics|April 1, 1989
Mapping the short arm of human chromosome 16D F Callen, V J Hyland, E G Baker, et al.
American Journal of Human Genetics|March 1, 1995
Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease)P E Taschner, N de Vos, A D Thompson, et al.
Gut|July 3, 2007
Somatic APC mosaicism: an underestimated cause of polyposis coliF J Hes, M Nielsen, E C Bik, et al.
Journal of Medical Genetics|October 1, 1990
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)M H Breuning, F G Snijdewint, H Brunner, et al.
American Journal of Human Genetics|February 1, 1993
Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspectsR C Hennekam, M Tilanus, B C Hamel, et al.
Pageof 40

Showing results (241-250 of 391) with videos related to

Sort By:
Pageof 40
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1992
Construction of a map of chromosome 16 by using radiation hybridsI Ceccherini, G Romeo, S Lawrence, et al.
European Journal of Human Genetics : EJHG|May 12, 2016
Analysis of mutations within the intron20 splice donor site of CREBBP in patients with and without classical RSTSJohannes G Dauwerse, Martine van Belzen, Arie van Haeringen, et al.
American Journal of Human Genetics|August 16, 2006
Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferaseSaskia A J Lesnik Oberstein, Marjolein Kriek, Stefan J White, et al.
British Journal of Cancer|May 29, 2003
Genetic counselling and the intention to undergo prophylactic mastectomy: effects of a breast cancer risk assessmentS van Dijk, W Otten, M W Zoeteweij, et al.
Journal of Dental Research|July 26, 2017
Orthodontics with Customized versus Noncustomized Appliances: A Randomized Controlled Clinical TrialE W Penning, R H J Peerlings, J D M Govers, et al.
Genomics|April 1, 1989
Mapping the short arm of human chromosome 16D F Callen, V J Hyland, E G Baker, et al.
American Journal of Human Genetics|March 1, 1995
Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease)P E Taschner, N de Vos, A D Thompson, et al.
Gut|July 3, 2007
Somatic APC mosaicism: an underestimated cause of polyposis coliF J Hes, M Nielsen, E C Bik, et al.
Journal of Medical Genetics|October 1, 1990
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1)M H Breuning, F G Snijdewint, H Brunner, et al.
American Journal of Human Genetics|February 1, 1993
Deletion at chromosome 16p13.3 as a cause of Rubinstein-Taybi syndrome: clinical aspectsR C Hennekam, M Tilanus, B C Hamel, et al.
Pageof 40