Implication of the Strand-Specific Imprinting and Segregation Model: Integrating in utero Hormone Exposure, Stem Cell and Lateral Asymmetry Hypotheses in Breast Cancer Aetiology

Known genetic mutations and familial hereditary factors account for less than 20–25% of breast cancer cases in women, therefore, most instances have been classified as sporadic cases of unknown aetiologies. Single nucleotide polymorphisms (SNPs) were considered as breast cancer risk factors, but num...

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Detalles Bibliográficos
Autores principales: Harbinder, Singh, Lazzara, Carol A, Klar, Amar JS
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478350/
https://www.ncbi.nlm.nih.gov/pubmed/34589269
http://dx.doi.org/10.4172/2161-1041.s2-005

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8478350/
https://www.ncbi.nlm.nih.gov/pubmed/34589269
http://dx.doi.org/10.4172/2161-1041.s2-005

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