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Citation: M. Bitner-glindzicz et al., A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene, NAT GENET, 26(1), 2000, pp. 56-60

Authors: Feather, SA Malcolm, S Woolf, AS Wright, V Blaydon, D Reid, CJD Flinter, FA Proesmans, W Devriendt, K Carter, J Warwicker, P Goodship, THJ Goodship, JA

Citation: Sa. Feather et al., Primary, nonsyndromic vesicoureteric reflux and its nephropathy is genetically heterogeneous, with a locus on chromosome 1, AM J HU GEN, 66(4), 2000, pp. 1420-1425