Authors:
Bitner-Glindzicz, M
Lindley, KJ
Rutland, P
Blaydon, D
Smith, VV
Milla, PJ
Hussain, K
Furth-Lavi, J
Cosgrove, KE
Shepherd, RM
Barnes, PD
O'Brien, RE
Farndon, PA
Sowden, J
Liu, XZ
Scanlan, MJ
Malcolm, S
Dunne, MJ
Aynsley-Green, A
Glaser, B
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