Paternal imprinting of the SLC22A1LS gene located in the human chromosome segment 11p15.5

BACKGROUND: Genomic imprinting is an epigenetic chromosomal modification in the gametes or zygotes that results in a non-random monoallelic expression of specific autosomal genes depending upon their parent of origin. Approximately 44 human genes have been reported to be imprinted. A majority of the...

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Detalles Bibliográficos
Autores principales: Bajaj, Vineeta, Markandaya, Manjunath, Krishna, Lingegowda, Kumar, Arun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC425576/
https://www.ncbi.nlm.nih.gov/pubmed/15175115
http://dx.doi.org/10.1186/1471-2156-5-13

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC425576/
https://www.ncbi.nlm.nih.gov/pubmed/15175115
http://dx.doi.org/10.1186/1471-2156-5-13

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