Authors:
WINDL O
DEMPSTER M
ESTIBEIRO JP
LATHE R
DESILVA R
ESMONDE T
WILL R
SPRINGBETT A
CAMPBELL TA
SIDLE KCL
PALMER MS
COLLINGE J
Citation: O. Windl et al., GENETIC-BASIS OF CREUTZFELDT-JAKOB-DISEASE IN THE UNITED-KINGDOM - A SYSTEMATIC ANALYSIS OF PREDISPOSING MUTATIONS AND ALLELIC VARIATION INTHE PRNP GENE, Human genetics, 98(3), 1996, pp. 259-264
Authors:
NICHOLL D
WINDL O
DESILVA R
SAWCER S
DEMPSTER M
IRONSIDE JW
ESTIBEIRO JP
YUILL GM
LATHE R
WILL RG
Citation: D. Nicholl et al., INHERITED CREUTZFELDT-JAKOB-DISEASE IN A BRITISH FAMILY ASSOCIATED WITH A NOVEL 144-BASE-PAIR INSERTION OF THE PRION PROTEIN GENE, Journal of Neurology, Neurosurgery and Psychiatry, 58(1), 1995, pp. 65-69
Authors:
DESILVA R
WINDL O
DEMPSTER M
ESTIBEIRO JP
ESMONDE T
LATHE R
IRONSIDE JW
WILL R
Citation: R. Desilva et al., PRION PROTEIN GENOTYPE IN CREUTZFELDT-JAKOB-DISEASE - THE EDINBURGH EXPERIENCE, Annals of neurology, 36(2), 1994, pp. 272-272
Citation: Fa. Brook et al., FEMALE PREDISPOSITION TO CRANIAL NEURAL-TUBE DEFECTS IS NOT BECAUSE OF A DIFFERENCE BETWEEN THE SEXES IN THE RATE OF EMBRYONIC GROWTH OR DEVELOPMENT DURING NEURULATION, Journal of Medical Genetics, 31(5), 1994, pp. 383-387
Citation: Jp. Estibeiro et al., INTERACTION BETWEEN SPLOTCH (SP) AND CURLY TAIL (CT) MOUSE MUTANTS INTHE EMBRYONIC-DEVELOPMENT OF NEURAL-TUBE DEFECTS, Development, 119(1), 1993, pp. 113-121