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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 8, 2023. (Total: 223870Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Abnormalities and SMARCB1[original query]
Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors.
Pediatric blood & cancer 2011 Jan 56 (1): 7-15.
Eaton Katherine W, Tooke Laura S, Wainwright Luanne M, Judkins Alexander R, Biegel Jaclyn
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,
Epithelial-Myoepithelial Carcinoma: Frequent Morphologic and Molecular Evidence of Preexisting Pleomorphic Adenoma, Common HRAS Mutations in PLAG1-intact and HMGA2-intact Cases, and Occasional TP53, FBXW7, and SMARCB1 Alterations in High-grade Cases.
The American journal of surgical pathology 2017 Nov .
El Hallani Soufiane, Udager Aaron M, Bell Diana, Fonseca Isabel, Thompson Lester D R, Assaad Adel, Agaimy Abbas, Luvison Alyssa M, Miller Caitlyn, Seethala Raja R, Chiosea Simi
Landscape of Cyclin Pathway Genomic Alterations Across 5,356 Prostate Cancers: Implications for Targeted Therapeutics.
The oncologist 2021 2 26 (4): e715-e718.
Jardim Denis L, Millis Sherri Z, Ross Jeffrey S, Woo Michelle Sue-Ann, Ali Siraj M, Kurzrock Razel
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