Authors: Henwood, J Pickard, C Leek, JP Bennett, CP Crow, YJ Thomson, JDR Ahmed, M Watterson, KG Parsons, JM Roberts, E Lench, NJ

Citation: J. Henwood et al., A region of homozygosity within 22q11.2 associated with congenital heart disease: recessive DiGeorge/velocardiofacial syndrome?, J MED GENET, 38(8), 2001, pp. 533-536

Authors: Pattison, L Crow, YJ Deeble, VJ Jackson, AP Jafri, H Rashid, Y Roberts, E Woods, CG

Citation: L. Pattison et al., A fifth locus for primary autosomal recessive microcephaly maps to chromosome 1q31, AM J HU GEN, 67(6), 2000, pp. 1578-1580

Authors: Crow, YJ Jackson, AP Roberts, E van Beusekom, E Barth, P Corry, P Ferrie, CD Hamel, BCJ Jayatunga, R Karbani, G Kalmanchey, R Kelemen, A King, M Kumar, R Livingstone, J Massey, R McWilliam, R Meager, A Rittey, C Stephenson, JBP Tolmie, JL Verrips, A Voit, T van Bokhoven, H Brunner, HG Woods, CG

Citation: Yj. Crow et al., Aicardi-Goutieres syndrome display genetic heterogeneity with one locus (AGS1) on chromosome 3p21, AM J HU GEN, 67(1), 2000, pp. 213-221

Authors: Stephenson, JBP Greene, NDE Leung, KY Munroe, PB Mole, SE Gardiner, RM Taschner, PEM O'Regan, M Naismith, K Crow, YJ Mitchison, HM

Citation: Jbp. Stephenson et al., The molecular basis of GROD-storing neuronal ceroid lipofuscinoses in Scotland, MOL GEN MET, 66(4), 1999, pp. 245-247