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3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.
Willatt L, Cox J, Barber J, Cabanas ED, Collins A, Donnai D, FitzPatrick DR, Maher E, Martin H, Parnau J, Pindar L, Ramsay J, Shaw-Smith C, Sistermans EA, Tettenborn M, Trump D, de Vries BB, Walker K, Raymond FL. Willatt L, et al. Among authors: tettenborn m. Am J Hum Genet. 2005 Jul;77(1):154-60. doi: 10.1086/431653. Epub 2005 May 25. Am J Hum Genet. 2005. PMID: 15918153 Free PMC article.
A new form of autosomal dominant arthrogryposis.
Lai MM, Tettenborn MA, Hall JG, Smith LJ, Berry AC. Lai MM, et al. Among authors: tettenborn ma. J Med Genet. 1991 Oct;28(10):701-3. doi: 10.1136/jmg.28.10.701. J Med Genet. 1991. PMID: 1941966 Free PMC article.
Food intolerance.
Anthony HM, Birtwistle S, Brostoff J, Eaton KK, Hearn G, Maberly DJ, Mansfield JR, Radcliffe M, Tettenborn M. Anthony HM, et al. Among authors: tettenborn m. Lancet. 1994 Jul 9;344(8915):136-7; author reply 137-8. Lancet. 1994. PMID: 7912378 No abstract available.