Connection
Kenneth MacLean to Syndrome
This is a "connection" page, showing publications Kenneth MacLean has written about Syndrome.
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0.116 |
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Maclean K, Holme SA, Gilmour E, Taylor M, Scheffer H, Graf N, Smith GH, Onikul E, van Bokhoven H, Moss C, Adès LC. EEC syndrome, Arg227Gln TP63 mutation and micturition difficulties: Is there a genotype-phenotype correlation? Am J Med Genet A. 2007 May 15; 143A(10):1114-9.
Score: 0.063
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Maclean K, Smith J, St Heaps L, Chia N, Williams R, Peters GB, Onikul E, McCrossin T, Lehmann OJ, Adès LC. Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome. Am J Med Genet A. 2005 Feb 01; 132A(4):381-5.
Score: 0.054