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H Brems

Showing results (11-20 of 19) with videos related to

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Clinical Genetics|October 8, 2016
Choroidal abnormalities in café-au-lait syndromes: a new differential diagnostic tool?C Cassiman, I Casteels, J Jacob, et al.
Human Reproduction (Oxford, England)|March 13, 2009
Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletionsE Vanneste, C Melotte, S Debrock, et al.
Human Mutation|October 26, 1999
Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletionsC Lopez Correa, H Brems, C Lázaro, et al.
American Journal of Human Genetics|March 28, 2003
Elevated risk for MPNST in NF1 microdeletion patientsT De Raedt, H Brems, P Wolkenstein, et al.
Acta Gastro-Enterologica Belgica|March 19, 2022
Prevalence of microsatellite instable and Epstein-Barr Virus-driven gastroesophageal cancer in a large Belgian cohortS De Meulder, X Sagaert, H Brems, et al.
Gynecologic Oncology|January 26, 2020
Analysis of 108 patients with endometrial carcinoma using the PROMISE classification and additional genetic analyses for MMR-DS Timmerman, A S Van Rompuy, T Van Gorp, et al.
Human Molecular Genetics|July 7, 2001
Recombination hotspot in NF1 microdeletion patientsC López-Correa, M Dorschner, H Brems, et al.
The New England Journal of Medicine|October 24, 2022
Oxygen-Saturation Targets for Critically Ill Adults Receiving Mechanical VentilationMatthew W Semler, Jonathan D Casey, Bradley D Lloyd, et al.
Science (New York, N.Y.)|November 17, 2018
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitinationM Steklov, S Pandolfi, M F Baietti, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Clinical Genetics|October 8, 2016
Choroidal abnormalities in café-au-lait syndromes: a new differential diagnostic tool?C Cassiman, I Casteels, J Jacob, et al.
Human Reproduction (Oxford, England)|March 13, 2009
Preimplantation genetic diagnosis using fluorescent in situ hybridization for cancer predisposition syndromes caused by microdeletionsE Vanneste, C Melotte, S Debrock, et al.
Human Mutation|October 26, 1999
Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletionsC Lopez Correa, H Brems, C Lázaro, et al.
American Journal of Human Genetics|March 28, 2003
Elevated risk for MPNST in NF1 microdeletion patientsT De Raedt, H Brems, P Wolkenstein, et al.
Acta Gastro-Enterologica Belgica|March 19, 2022
Prevalence of microsatellite instable and Epstein-Barr Virus-driven gastroesophageal cancer in a large Belgian cohortS De Meulder, X Sagaert, H Brems, et al.
Gynecologic Oncology|January 26, 2020
Analysis of 108 patients with endometrial carcinoma using the PROMISE classification and additional genetic analyses for MMR-DS Timmerman, A S Van Rompuy, T Van Gorp, et al.
Human Molecular Genetics|July 7, 2001
Recombination hotspot in NF1 microdeletion patientsC López-Correa, M Dorschner, H Brems, et al.
The New England Journal of Medicine|October 24, 2022
Oxygen-Saturation Targets for Critically Ill Adults Receiving Mechanical VentilationMatthew W Semler, Jonathan D Casey, Bradley D Lloyd, et al.
Science (New York, N.Y.)|November 17, 2018
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitinationM Steklov, S Pandolfi, M F Baietti, et al.
Pageof 2