Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen

BACKGROUND: The phenotypic heterogeneity of sickle cell disease is likely the result of multiple genetic factors and their interaction with the sickle mutation. High transcranial doppler (TCD) velocities define a subgroup of children with sickle cell disease who are at increased risk for developing...

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Detalles Bibliográficos
Autores principales: Adams, Gaye T, Snieder, Harold, McKie, Virgil C, Clair, Betsy, Brambilla, Donald, Adams, Robert J, Kutlar, Ferdane, Kutlar, Abdullah
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Study Protocol
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC183831/
https://www.ncbi.nlm.nih.gov/pubmed/12871600
http://dx.doi.org/10.1186/1471-2350-4-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC183831/
https://www.ncbi.nlm.nih.gov/pubmed/12871600
http://dx.doi.org/10.1186/1471-2350-4-6

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