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Review
. 1998 Dec;33(6):928-9.
doi: 10.1007/s005350050207.

Lack of chromosome 15q11-q13 region involvement in a family with Cowden disease/Bannayan-Zonana syndrome

M J Dasouki, A Marney, M G Butler
Review

Lack of chromosome 15q11-q13 region involvement in a family with Cowden disease/Bannayan-Zonana syndrome

M J Dasouki et al. J Gastroenterol. 1998 Dec.
No abstract available

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References

    1. Suzuki T, Ichinose M, Matsubara Y, et al. Cowden’s disease with a defined genetic alteration-chromosomal duplication at 15ql1-ql3. J Gastroenterol 1997;32:696–699. - PubMed
    1. Arch EM, Goodman BK, Van W esep RA, et al. Deletion of PTEN in a patient with Bannayan-Riley-Ruvalcaba syndrome suggests allelism with Cowden disease. Am J Med Genet 1997;71:489–493. - PubMed
    1. Christian SL, Robinson WP, Huang B, et al. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelm an syndrome patients. Am J Hum Genet 1995;57:40–48. - PMC - PubMed
    1. Israel J, Lessick M, Szego K, et al. Translocation 19; Y in a child with Bannayan-Zonana phenotype. J Med Genet 1991:28:427–428. - PMC - PubMed
    1. Tsuchiya KD. Wiesner G, Cassidy SB, et al. Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome. Genes Chromosom Cancer 1998:21:113–118. - PubMed

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