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John Burn

Showing results (141-150 of 162) with videos related to

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Gut|February 15, 2013
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European expertsHans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, et al.
The Journal of Allergy and Clinical Immunology|October 3, 2013
Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjectsSean P Saunders, Christabelle S M Goh, Sara J Brown, et al.
Hereditary Cancer in Clinical Practice|October 20, 2017
Colorectal cancer incidence in <i>path_MLH1</i> carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database reportToni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, et al.
American Journal of Human Genetics|December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndromeDagmar Wieczorek, William G Newman, Thomas Wieland, et al.
Human Mutation|July 4, 2012
Human Variome Project country nodes: documenting genetic information within a countryGeorge P Patrinos, Timothy D Smith, Heather Howard, et al.
Gut|July 30, 2017
Cancer risk and survival in <i>path_MMR</i> carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome DatabasePål Møller, Toni T Seppälä, Inge Bernstein, et al.
Journal of Personalized Medicine|April 23, 2022
Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 CountriesBin Hashim Halim-Fikri, Carsten W Lederer, Atif Amin Baig, et al.
Gastroenterology|December 31, 2022
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair DeficiencyRichard Gallon, Rachel Phelps, Christine Hayes, et al.
Journal of Medical Genetics|December 26, 2022
Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996-2020: development of a national resource of patient-level genomics laboratory recordsLucy Loong, Catherine Huntley, Fiona McRonald, et al.
Hereditary Cancer in Clinical Practice|October 23, 2019
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database reportMev Dominguez-Valentin, Toni T Seppälä, Julian R Sampson, et al.
Pageof 17

Showing results (141-150 of 162) with videos related to

Sort By:
Pageof 17
Gut|February 15, 2013
Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European expertsHans F A Vasen, Ignacio Blanco, Katja Aktan-Collan, et al.
The Journal of Allergy and Clinical Immunology|October 3, 2013
Tmem79/Matt is the matted mouse gene and is a predisposing gene for atopic dermatitis in human subjectsSean P Saunders, Christabelle S M Goh, Sara J Brown, et al.
Hereditary Cancer in Clinical Practice|October 20, 2017
Colorectal cancer incidence in <i>path_MLH1</i> carriers subjected to different follow-up protocols: a Prospective Lynch Syndrome Database reportToni Seppälä, Kirsi Pylvänäinen, Dafydd Gareth Evans, et al.
American Journal of Human Genetics|December 1, 2014
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndromeDagmar Wieczorek, William G Newman, Thomas Wieland, et al.
Human Mutation|July 4, 2012
Human Variome Project country nodes: documenting genetic information within a countryGeorge P Patrinos, Timothy D Smith, Heather Howard, et al.
Gut|July 30, 2017
Cancer risk and survival in <i>path_MMR</i> carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome DatabasePål Møller, Toni T Seppälä, Inge Bernstein, et al.
Journal of Personalized Medicine|April 23, 2022
Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 CountriesBin Hashim Halim-Fikri, Carsten W Lederer, Atif Amin Baig, et al.
Gastroenterology|December 31, 2022
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair DeficiencyRichard Gallon, Rachel Phelps, Christine Hayes, et al.
Journal of Medical Genetics|December 26, 2022
Germline mismatch repair (MMR) gene analyses from English NHS regional molecular genomics laboratories 1996-2020: development of a national resource of patient-level genomics laboratory recordsLucy Loong, Catherine Huntley, Fiona McRonald, et al.
Hereditary Cancer in Clinical Practice|October 23, 2019
Survival by colon cancer stage and screening interval in Lynch syndrome: a prospective Lynch syndrome database reportMev Dominguez-Valentin, Toni T Seppälä, Julian R Sampson, et al.
Pageof 17