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Estelle Chanudet

Showing results (21-30 of 27) with videos related to

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Brain : a Journal of Neurology|September 12, 2013
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomaliesEmma A Webb, Angham AlMutair, Daniel Kelberman, et al.
Journal of Medical Genetics|January 8, 2015
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypesAoife M Waters, Rowan Asfahani, Paula Carroll, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 23, 2023
Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell CarcinomaNaveen S Vasudev, Ghislaine Scelo, Kate I Glennon, et al.
Nature Genetics|October 19, 2021
Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidenceSarah Moody, Sergey Senkin, S M Ashiqul Islam, et al.
Cell Genomics|February 7, 2024
The Mutographs biorepository: A unique genomic resource to study cancer around the worldSandra Perdomo, Behnoush Abedi-Ardekani, Ana Carolina de Carvalho, et al.
Nature|May 1, 2024
Geographic variation of mutagenic exposures in kidney cancer genomesSergey Senkin, Sarah Moody, Marcos Díaz-Gay, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
Brain : a Journal of Neurology|September 12, 2013
ARNT2 mutation causes hypopituitarism, post-natal microcephaly, visual and renal anomaliesEmma A Webb, Angham AlMutair, Daniel Kelberman, et al.
Journal of Medical Genetics|January 8, 2015
The kinetochore protein, CENPF, is mutated in human ciliopathy and microcephaly phenotypesAoife M Waters, Rowan Asfahani, Paula Carroll, et al.
American Journal of Human Genetics|December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndromeAnna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 23, 2023
Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell CarcinomaNaveen S Vasudev, Ghislaine Scelo, Kate I Glennon, et al.
Nature Genetics|October 19, 2021
Mutational signatures in esophageal squamous cell carcinoma from eight countries with varying incidenceSarah Moody, Sergey Senkin, S M Ashiqul Islam, et al.
Cell Genomics|February 7, 2024
The Mutographs biorepository: A unique genomic resource to study cancer around the worldSandra Perdomo, Behnoush Abedi-Ardekani, Ana Carolina de Carvalho, et al.
Nature|May 1, 2024
Geographic variation of mutagenic exposures in kidney cancer genomesSergey Senkin, Sarah Moody, Marcos Díaz-Gay, et al.
Pageof 3