Complementation Analysis in Fanconi Anemia: Assignment of the Reference FA-H Patient to Group A

Fanconi anemia (FA) is an autosomal recessive disorder with diverse clinical symptoms and extensive genetic heterogeneity. Of eight FA genes that have been implicated on the basis of complementation studies, four have been identified and two have been mapped to different loci; the status of the gene...

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Main Authors: Joenje, Hans, Levitus, Marieke, Waisfisz, Quinten, D’Andrea, Alan, Garcia-Higuera, Irene, Pearson, Tommy, van Berkel, Carola G. M., Rooimans, Martin A., Morgan, Neil, Mathew, Christopher G., Arwert, Fré
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society of Human Genetics 2000
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1287536/
https://ncbi.nlm.nih.gov/pubmed/10936108
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