SNPitty
Author:
Publisher
Elsevier BV
Subject
Molecular Medicine,Pathology and Forensic Medicine
Reference33 articles.
1. Hallmarks of cancer: the next generation;Hanahan;Cell,2011
2. Pan-cancer patterns of somatic copy number alteration;Zack;Nat Genet,2013
3. Patterns and functional implications of rare germline variants across 12 cancer types;Lu;Nat Commun,2015
4. Mutations of the KIT gene and loss of heterozygosity of the PTEN region in a primary malignant melanoma arising from a mature cystic teratoma of the ovary;Tate;Cancer Genet Cytogenet,2009
5. Mechanisms underlying losses of heterozygosity in human colorectal cancers;Thiagalingam;Proc Natl Acad Sci U S A,2001
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1. Prevalence, clinical and molecular characteristics of early stage EGFR-mutated lung cancer in a real-life West-European cohort: Implications for adjuvant therapy;European Journal of Cancer;2023-03
2. Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in SAMD9L-Associated Neuropathy;Genes;2022-12-14
3. Molecular testing in metastatic basal cell carcinoma;Journal of the American Academy of Dermatology;2021-11
4. Malignant transformation of salivary gland pleomorphic adenoma: proof of principle;The Journal of Pathology: Clinical Research;2021-05-07
5. Case Report: Complete Maternal Uniparental Isodisomy of Chromosome 5 (iUPD(5)mat) With PCSK1 Nonsense Variant in an Infant With Recurrent Diarrhea;Frontiers in Genetics;2021-05-06
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