Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Abnormalities and SMARCA4[original query] |
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Genotype-phenotype correlation of Coffin-Siris syndrome caused by mutations in SMARCB1, SMARCA4, SMARCE1, and ARID1A. American journal of medical genetics. Part C, Seminars in medical genetics 2014 Sep 166C (3): 262-75. Kosho Tomoki, Okamoto Nobuhiko, |
A population-based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patients. Genes, chromosomes & cancer 2015 May 54 (5): 326-33. Dirse Vaidas, Bertasiute Agne, Gineikiene Egle, Zvirblis Tadas, Dambrauskiene Ruta, Gerbutavicius Rolandas, Juozaityte Elona, Malciute Ligita, Paulsson Kajsa, Griskevicius Laimon |
Common cancer-driver mutations and their association with abnormally methylated genes in lung adenocarcinoma from never-smokers. Lung cancer (Amsterdam, Netherlands) 2018 8 123 99-106. Tessema Mathewos, Rossi Michael R, Picchi Maria A, Yingling Christin M, Lin Yong, Ramalingam Suresh S, Belinsky Steven |
Metastatic grade 1 meningioma lacking genetic abnormalities commonly associated with bad prognosis. Pathology, research and practice 2022 Aug 238 154089. Barresi Valeria, Lawlor Rita T, Mafficini Andrea, Gilioli Eliana, Scarpa Al |
Lung cancer presenting with central nervous system metastasis: Clinicopathological and molecular analysis of 171 cases. Annals of diagnostic pathology 2023 1 63 152082. Demleitner Madeleine, Erlenbach-Wünsch Katharina, Coras Roland, Erber Ramona, Polifka Iris, Eyüpo?lu Ilker, Fuchs Florian, Hartmann Arndt, Agaimy Abb |
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- Page last updated:May 06, 2024
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