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Eric Legius

Showing results (41-50 of 165) with videos related to

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BMC Medical Genetics|May 1, 2015
Keratinocytic epidermal nevus syndrome with Schwann cell proliferation, lipomatous tumour and mosaic KRAS mutationSaid Farschtschi, Victor-Felix Mautner, Silke Hollants, et al.
Genetic Testing|April 29, 2005
Predictive testing for hereditary nonpolyposis colorectal cancer: subjective perception regarding colorectal and endometrial cancer, distress, and health-related behavior at one year post-testErna Claes, Lieve Denayer, Gerry Evers-Kiebooms, et al.
American Journal of Medical Genetics. Part A|October 19, 2010
Clinical and hematologic findings in Noonan syndrome patients with PTPN11 gene mutationsMurat Derbent, Yekta Öncel, Kürşad Tokel, et al.
BMC Medical Genetics|October 16, 2015
Mutation in NRAS in familial Noonan syndrome--case report and review of the literatureSara Ekvall, Maria Wilbe, Jovanna Dahlgren, et al.
Genes, Chromosomes & Cancer|June 27, 2013
EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletionMarijke Spaepen, Esther Neven, Xavier Sagaert, et al.
Journal of Mother and Child|March 8, 2021
A Patient with neonatal cholestasisKristl G Claeys, Luc Breysem, Eric Legius, et al.
Human Mutation|January 12, 2005
Large deletions of the APC gene in 15% of mutation-negative patients with classical polyposis (FAP): a Belgian studyGeneviève Michils, Sabine Tejpar, Reinhilde Thoelen, et al.
Human Mutation|October 6, 2009
Recurrent copy number alterations in BRCA1-mutated ovarian tumors alter biological pathwaysKarin Leunen, Olivier Gevaert, Anneleen Daemen, et al.
Pediatric Dermatology|March 2, 2018
Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA)-related overgrowth spectrum: A brief reportPieter Denorme, Marie-Anne Morren, Silke Hollants, et al.
American Journal of Human Genetics|August 2, 2007
Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1Ophélia Maertens, Sofie De Schepper, Jo Vandesompele, et al.
Pageof 17

Showing results (41-50 of 165) with videos related to

Sort By:
Pageof 17
BMC Medical Genetics|May 1, 2015
Keratinocytic epidermal nevus syndrome with Schwann cell proliferation, lipomatous tumour and mosaic KRAS mutationSaid Farschtschi, Victor-Felix Mautner, Silke Hollants, et al.
Genetic Testing|April 29, 2005
Predictive testing for hereditary nonpolyposis colorectal cancer: subjective perception regarding colorectal and endometrial cancer, distress, and health-related behavior at one year post-testErna Claes, Lieve Denayer, Gerry Evers-Kiebooms, et al.
American Journal of Medical Genetics. Part A|October 19, 2010
Clinical and hematologic findings in Noonan syndrome patients with PTPN11 gene mutationsMurat Derbent, Yekta Öncel, Kürşad Tokel, et al.
BMC Medical Genetics|October 16, 2015
Mutation in NRAS in familial Noonan syndrome--case report and review of the literatureSara Ekvall, Maria Wilbe, Jovanna Dahlgren, et al.
Genes, Chromosomes & Cancer|June 27, 2013
EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletionMarijke Spaepen, Esther Neven, Xavier Sagaert, et al.
Journal of Mother and Child|March 8, 2021
A Patient with neonatal cholestasisKristl G Claeys, Luc Breysem, Eric Legius, et al.
Human Mutation|January 12, 2005
Large deletions of the APC gene in 15% of mutation-negative patients with classical polyposis (FAP): a Belgian studyGeneviève Michils, Sabine Tejpar, Reinhilde Thoelen, et al.
Human Mutation|October 6, 2009
Recurrent copy number alterations in BRCA1-mutated ovarian tumors alter biological pathwaysKarin Leunen, Olivier Gevaert, Anneleen Daemen, et al.
Pediatric Dermatology|March 2, 2018
Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA)-related overgrowth spectrum: A brief reportPieter Denorme, Marie-Anne Morren, Silke Hollants, et al.
American Journal of Human Genetics|August 2, 2007
Molecular dissection of isolated disease features in mosaic neurofibromatosis type 1Ophélia Maertens, Sofie De Schepper, Jo Vandesompele, et al.
Pageof 17