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European Journal of Human Genetics : EJHG|October 16, 2014
Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinomaJean-Benoît Courcet, Siham Chafai Elalaoui, Laurence Duplomb, et al.
American Journal of Epidemiology|December 25, 2003
Pooled analysis of alcohol dehydrogenase genotypes and head and neck cancer: a HuGE reviewPaul Brennan, Sarah Lewis, Mia Hashibe, et al.
The Journal of Pathology|March 17, 2012
CDKN2A homozygous deletion is associated with muscle invasion in FGFR3-mutated urothelial bladder carcinomaSandra Rebouissou, Aurélie Hérault, Eric Letouzé, et al.
Frontiers in Genetics|February 3, 2022
XPC and POLH/XPV Genes Mutated in a Genetic Cluster of Xeroderma Pigmentosum Patients in Northeast BrazilLigia Pereira Castro, Danilo Batista-Vieira, Tiago Antonio de Souza, et al.
Carcinogenesis|May 17, 2023
Mutational signatures and increased retrotransposon insertions in xeroderma pigmentosum variant skin tumorsCamila Corradi, Juliana B Vilar, Vanessa C Buzatto, et al.
International Journal of Cancer|January 22, 2004
Secondhand smoke exposure in adulthood and risk of lung cancer among never smokers: a pooled analysis of two large studiesPaul Brennan, Patricia A Buffler, Peggy Reynolds, et al.
American Journal of Human Genetics|August 3, 2019
Bi-allelic TARS Mutations Are Associated with Brittle Hair PhenotypeArjan F Theil, Elena Botta, Anja Raams, et al.
Nature Communications|June 18, 2021
BRN2 is a non-canonical melanoma tumor-suppressorMichael Hamm, Pierre Sohier, Valérie Petit, et al.
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