PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

Marsh, D. et al. (1999) PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Human Molecular Genetics, 8(8), pp. 1461-1472.

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Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Ahmed, Professor Syed Faisal
Authors: Marsh, D., Kum, J., Lunetta, K., Bennett, M., Gorlin, R., Ahmed, S., Bodurtha, J., Crowe, C., Curtis, M., Dasouki, M., Dunn, T., Feit, H., Geraghty, M., Graham, J., Hodgson, S., Hunter, A., Korf, B., Manchester, D., Miesfeldt, S., Murday, V., Nathanson, K., Parisi, M., and Pober, B.
College/School:College of Medical Veterinary and Life Sciences
Journal Name:Human Molecular Genetics

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