Authors: WILLIAMS NM REES MI NORTON N HOLMANS P FENTON I CARDNO AG MURPHY KC JONES LA MCCARTHY G SANDERS R MCGUFFIN P OWEN MJ

Citation: Nm. Williams et al., A 2-STAGE SIB-PAIR GENOME SCAN FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES, American journal of medical genetics, 81(6), 1998, pp. 453-453

Authors: NORTON N WILLIAMS NM REES MI HOLMANS P FENTON I CARDNO AC MURPHY KC JONES LA SANDERS RD ASHERSON P MCGUFFIN P OWEN MJ

Citation: N. Norton et al., AN AFFECTED SIB PAIR STUDY FOR SCHIZOPHRENIA ON THE X-CHROMOSOME, American journal of medical genetics, 81(6), 1998, pp. 529-529

Authors: CARDNO AG HOLMANS PA JONES LA REES MI MURPHY KC WILLIAMS NM SANDERS RS FENTON I MCGUFFIN P OWEN MJ

Citation: Ag. Cardno et al., A SYSTEMATIC SEARCH FOR GENES DETERMINING AGE-OF-ONSET IN SCHIZOPHRENIA, American journal of medical genetics, 81(6), 1998, pp. 530-530

Authors: WILLIAMS NM REES MI HOLMANS P DANIELS J FENTON I CARDNO AG MURPHY KC JONES LA ASHERSON P MCGUFFIN P OWEN MJ

Citation: Nm. Williams et al., GENOME SEARCH FOR SCHIZOPHRENIA SUSCEPTIBILITY GENES USING A 2-STAGE SIB-PAIR APPROACH, American journal of medical genetics, 74(6), 1997, pp. 559-559

Authors: REES MI ANDREW M JAWAD S OWEN MJ

Citation: Mi. Rees et al., EVIDENCE FOR RECESSIVE AS WELL AS DOMINANT FORMS OF STARTLE DISEASE (HYPEREKPLEXIA) CAUSED BY MUTATIONS IN THE OR, SUBUNIT OF THE INHIBITORY GLYCINE RECEPTOR, Human molecular genetics, 3(12), 1994, pp. 2175-2179

Authors: REES MI WORWOOD M THOMPSON PW GILBERTSON C MAY A

Citation: Mi. Rees et al., RED-CELL DIMORPHISM IN A YOUNG MAN WITH A CONSTITUTIONAL CHROMOSOMAL TRANSLOCATION T(1122)(P15.5Q11.21), British Journal of Haematology, 87(2), 1994, pp. 386-395