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Hormones & Cancer|August 11, 2020
Prevalence of Histological Characteristics of Breast Cancer in Rwanda in Relation to Age and Tumor StagesJeanne P Uyisenga, Yvan Butera, Ahmed Debit, et al.
International Journal of Molecular Sciences|February 26, 2022
Novel Loss of Function Variant in BCKDK Causes a Treatable Developmental and Epileptic EncephalopathyFrançois Boemer, Claire Josse, Géraldine Luis, et al.
Journal of Personalized Medicine|June 27, 2024
Digenic Inheritance of Mutations in Homologous Recombination Genes in Cancer PatientsMaria Valeria Freire, Marie Martin, Karin Segers, et al.
Genes, Chromosomes & Cancer|July 26, 2016
Genomic studies of multiple myeloma reveal an association between X chromosome alterations and genomic profile complexityTiberio Sticca, Jean-Hubert Caberg, Stephane Wenric, et al.
Clinical Genetics|May 8, 2020
GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndromeAdeline Jacquinet, Bouchra Boujemla, Corinne Fasquelle, et al.
Journal of Inherited Metabolic Disease|May 15, 2015
Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophyFrançois-Guillaume Debray, Claudia Stümpfig, Arnaud V Vanlander, et al.
Oncotarget|January 7, 2016
Circulating microRNA-based screening tool for breast cancerPierre Frères, Stéphane Wenric, Meriem Boukerroucha, et al.
Oncology Letters|November 4, 2024
Genetic evaluation of patients with multiple primary cancersMaria Valeria Freire, Romain Thissen, Marie Martin, et al.
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