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Martijn H Breuning

Showing results (91-100 of 112) with videos related to

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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 5, 2008
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma familiesFemke A de Snoo, D Timothy Bishop, Wilma Bergman, et al.
Familial Cancer|March 15, 2016
Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registryHans F A Vasen, Mary E Velthuizen, Jan H Kleibeuker, et al.
Hormone Research in Paediatrics|October 11, 2014
Copy number variants in short children born small for gestational ageJan M Wit, Hermine A van Duyvenvoorde, Jan B van Klinken, et al.
Human Mutation|July 31, 2010
Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2Emmelien Aten, Lisa C Brasz, Dorothea Bornholdt, et al.
Breast Cancer Research and Treatment|February 3, 2012
MUTYH gene variants and breast cancer in a Dutch case–control studyAstrid A Out, Marijke Wasielewski, Petra E A Huijts, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma familiesFemke A de Snoo, Jouke-Jan Hottenga, Elizabeth M Gillanders, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Human Mutation|October 21, 2009
Deep sequencing to reveal new variants in pooled DNA samplesAstrid A Out, Ivonne J H M van Minderhout, Jelle J Goeman, et al.
Human Mutation|February 19, 2013
Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease)Yu Sun, Rowida Almomani, Guido J Breedveld, et al.
Pageof 12

Showing results (91-100 of 112) with videos related to

Sort By:
Pageof 12
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 5, 2008
Increased risk of cancer other than melanoma in CDKN2A founder mutation (p16-Leiden)-positive melanoma familiesFemke A de Snoo, D Timothy Bishop, Wilma Bergman, et al.
Familial Cancer|March 15, 2016
Hereditary cancer registries improve the care of patients with a genetic predisposition to cancer: contributions from the Dutch Lynch syndrome registryHans F A Vasen, Mary E Velthuizen, Jan H Kleibeuker, et al.
Hormone Research in Paediatrics|October 11, 2014
Copy number variants in short children born small for gestational ageJan M Wit, Hermine A van Duyvenvoorde, Jan B van Klinken, et al.
Human Mutation|July 31, 2010
Keratosis Follicularis Spinulosa Decalvans is caused by mutations in MBTPS2Emmelien Aten, Lisa C Brasz, Dorothea Bornholdt, et al.
Breast Cancer Research and Treatment|February 3, 2012
MUTYH gene variants and breast cancer in a Dutch case–control studyAstrid A Out, Marijke Wasielewski, Petra E A Huijts, et al.
European Journal of Human Genetics : EJHG|April 10, 2008
Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma familiesFemke A de Snoo, Jouke-Jan Hottenga, Elizabeth M Gillanders, et al.
American Journal of Human Genetics|October 25, 2011
Craniosynostosis and multiple skeletal anomalies in humans and zebrafish result from a defect in the localized degradation of retinoic acidKathrin Laue, Hans-Martin Pogoda, Philip B Daniel, et al.
Gastroenterology|February 14, 2006
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome)Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, et al.
Human Mutation|October 21, 2009
Deep sequencing to reveal new variants in pooled DNA samplesAstrid A Out, Ivonne J H M van Minderhout, Jelle J Goeman, et al.
Human Mutation|February 19, 2013
Autosomal recessive spinocerebellar ataxia 7 (SCAR7) is caused by variants in TPP1, the gene involved in classic late-infantile neuronal ceroid lipofuscinosis 2 disease (CLN2 disease)Yu Sun, Rowida Almomani, Guido J Breedveld, et al.
Pageof 12