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Quarterly Journal of the Royal Meteorological Society. Royal Meteorological Society (Great Britain)
|
December 3, 2019
Current state of the global operational aerosol multi-model ensemble: An update from the International Cooperative for Aerosol Prediction (ICAP)
Peng Xian, Jeffrey S Reid, Edward J Hyer, et al.
European Journal of Human Genetics : EJHG
|
August 11, 2011
People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population
Bruce Winney, Abdelhamid Boumertit, Tammy Day, et al.
Hereditary Cancer in Clinical Practice
|
May 13, 2024
Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated "Big Bang" pathway to CRC in three of the four Lynch syndromes
Pål Møller, Saskia Haupt, Aysel Ahadova, et al.
Gut
|
April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposis
K Woodford-Richens, S Bevan, M Churchman, et al.
Molecular Cancer Research : MCR
|
March 28, 2024
PIGA Mutations and Glycosylphosphatidylinositol Anchor Dysregulation in Polyposis-Associated Duodenal Tumorigenesis
Elena Meuser, Kyle Chang, Angharad Walters, et al.
Nature Communications
|
July 8, 2022
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells
Philip S Robinson, Laura E Thomas, Federico Abascal, et al.
Pediatric Neurology
|
August 16, 2021
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations
Hope Northrup, Mary E Aronow, E Martina Bebin, et al.
Gut
|
January 16, 2008
Guidelines for the clinical management of familial adenomatous polyposis (FAP)
H F A Vasen, G Möslein, A Alonso, et al.
Gut
|
June 29, 2010
Peutz-Jeghers syndrome: a systematic review and recommendations for management
A D Beggs, A R Latchford, H F A Vasen, et al.
Nature Communications
|
January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness
S Kmoch, J Majewski, V Ramamurthy, et al.
Page
of 52
Search research articles
Search
Showing results (481-490 of 518) with videos related to
Sort By:
Page
of 52
Quarterly Journal of the Royal Meteorological Society. Royal Meteorological Society (Great Britain)
|
December 3, 2019
Current state of the global operational aerosol multi-model ensemble: An update from the International Cooperative for Aerosol Prediction (ICAP)
Peng Xian, Jeffrey S Reid, Edward J Hyer, et al.
European Journal of Human Genetics : EJHG
|
August 11, 2011
People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population
Bruce Winney, Abdelhamid Boumertit, Tammy Day, et al.
Hereditary Cancer in Clinical Practice
|
May 13, 2024
Incidences of colorectal adenomas and cancers under colonoscopy surveillance suggest an accelerated "Big Bang" pathway to CRC in three of the four Lynch syndromes
Pål Møller, Saskia Haupt, Aysel Ahadova, et al.
Gut
|
April 15, 2000
Analysis of genetic and phenotypic heterogeneity in juvenile polyposis
K Woodford-Richens, S Bevan, M Churchman, et al.
Molecular Cancer Research : MCR
|
March 28, 2024
PIGA Mutations and Glycosylphosphatidylinositol Anchor Dysregulation in Polyposis-Associated Duodenal Tumorigenesis
Elena Meuser, Kyle Chang, Angharad Walters, et al.
Nature Communications
|
July 8, 2022
Inherited MUTYH mutations cause elevated somatic mutation rates and distinctive mutational signatures in normal human cells
Philip S Robinson, Laura E Thomas, Federico Abascal, et al.
Pediatric Neurology
|
August 16, 2021
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations
Hope Northrup, Mary E Aronow, E Martina Bebin, et al.
Gut
|
January 16, 2008
Guidelines for the clinical management of familial adenomatous polyposis (FAP)
H F A Vasen, G Möslein, A Alonso, et al.
Gut
|
June 29, 2010
Peutz-Jeghers syndrome: a systematic review and recommendations for management
A D Beggs, A R Latchford, H F A Vasen, et al.
Nature Communications
|
January 10, 2015
Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness
S Kmoch, J Majewski, V Ramamurthy, et al.
Page
of 52