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Stage-specific apoptosis, developmental delay, and embryonic lethality in mice homozygous for a targeted disruption in the murine Bloom’s syndrome gene

Bloom’s syndrome is a human autosomal genetic disorder characterized at the cellular level by genome instability and increased sister chomatid exchanges (SCEs). Clinical features of the disease include proportional dwarfism and a predisposition to develop a wide variety of malignancies. The human BL...

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Autores principales: Chester, Nicholas, Kuo, Frank, Kozak, Christine, O’Hara, Cathie D., Leder, Philip
Formato: Artigo
Lenguaje:Inglês
Publicado: Cold Spring Harbor Laboratory Press 1998
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC317228/
https://ncbi.nlm.nih.gov/pubmed/9808625
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