Authors:
Rees, MI
Lewis, TM
Vafa, B
Ferrie, C
Corry, P
Muntoni, F
Jungbluth, H
Stephenson, JBP
Kerr, M
Snell, RG
Schofield, RR
Owen, MJ
Citation: Mi. Rees et al., Compound heterozygosity and nonsense mutations in the alpha(1)-subunit of the inhibitory glycine receptor in hyperekplexia, HUM GENET, 109(3), 2001, pp. 267-270
Authors:
Cardno, AG
Holmans, PA
Rees, MI
Jones, LA
McCarthy, GM
Hamshere, ML
Williams, NM
Norton, N
Williams, HJ
Fenton, I
Murphy, KC
Sanders, RD
Gray, MY
O'Donovan, MC
McGuffin, P
Owen, MJ
Citation: Ag. Cardno et al., A genomewide linkage study of age at onset in schizophrenia, AM J MED G, 105(5), 2001, pp. 439-445
Authors:
Baker, KL
Rees, MI
Thompson, PW
Howell, RT
Cole, TR
Hughes, HE
Upadhyaya, M
Ravine, D
Citation: Kl. Baker et al., Chromosome 2 interstitial deletion (del(2) (q14.1q21)) associated with connective tissue laxity and an attention deficit disorder, J MED GENET, 38(7), 2001, pp. 493-496
Authors:
Rees, MI
Watts, P
Fenton, I
Clarke, A
Snell, RG
Owen, MJ
Gray, J
Citation: Mi. Rees et al., Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA(3)), HUM GENET, 106(2), 2000, pp. 206-209
Authors:
Rees, MI
Fenton, I
Williams, NM
Holmans, P
Norton, N
Cardno, A
Asherson, P
Spurlock, G
Roberts, E
Parfitt, E
Mant, P
Vallada, H
Dawson, E
Li, MW
Collier, DA
Powell, JF
Nanko, S
Gill, M
McGuffin, P
Owen, MJ
Citation: Mi. Rees et al., Autosome search for schizophrenia susceptibility genes in multiply affected families, MOL PSYCHI, 4(4), 1999, pp. 353-359
Authors:
Williams, NM
Rees, MI
Holmans, P
Norton, N
Cardno, AG
Jones, LA
Murphy, KC
Sanders, RD
McCarthy, G
Gray, MY
Fenton, I
McGuffin, P
Owen, MJ
Citation: Nm. Williams et al., A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs, HUM MOL GEN, 8(9), 1999, pp. 1729-1739