Authors:
GOOSSENS D
HARDING B
RAEYMAEKERS P
VANBROECKHOVEN C
DELFAVERO J
Citation: D. Goossens et al., REGION-SPECIFIC ISOLATION AND CHARACTERIZATION OF TRIPLET REPEATS, American journal of medical genetics, 81(6), 1998, pp. 468-469
Authors:
BASSETT JHD
FORBES SA
PANNETT AAJ
LLOYD SE
CHRISTIE PT
WOODING C
EDWARDS CR
MONSON JP
SAMPSON J
WASS JAH
HARDING B
BESSER GM
WHEELER MH
THAKKER RV
Citation: Jhd. Bassett et al., CHARACTERIZATION OF MUTATIONS IN PATIENTS WITH MULTIPLE ENDOCRINE NEOPLASIA TYPE-1, American journal of human genetics, 62(2), 1998, pp. 232-244
Citation: D. Ellison et al., KI-67 LABELING INDEX IS A PROGNOSTIC INDICATOR IN CHILDHOOD POSTERIOR-FOSSA EPENDYMOMA, Brain pathology, 7(4), 1997, pp. 1190-1190
Authors:
FORBES SA
PANNETT AAJ
BASSETT JHD
HARDING B
WOODING C
THAKKER RV
BUTLER R
OGILVIE D
ANAND R
GAUDRAY P
WEBER G
LARSSON C
ZHANG CX
CALENDER A
HOPPENER JWM
LIPS CJM
KAS K
Citation: Sa. Forbes et al., MAPPING OF THE GENE ENCODING THE B56-BETA SUBUNIT OF PROTEIN PHOSPHATASE 2A (PPP2R5B) TO A 0.5-MB REGION OF CHROMOSOME 11Q13 AND ITS EXCLUSION AS A CANDIDATE GENE FOR MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 (MEN1), Human genetics, 100(3-4), 1997, pp. 481-485
Authors:
STAPLETON SR
DAVID KM
HARKNESS WFJ
HARDING B
Citation: Sr. Stapleton et al., CENTRAL NEUROCYTOMA OF THE CERVICAL SPINAL-CORD, Journal of Neurology, Neurosurgery and Psychiatry, 63(1), 1997, pp. 119-119
Authors:
PANG JT
LLOYD SE
WOODING C
FARREN B
POTTINGER B
HARDING B
LEIGH SEA
POOK MA
BENHAM FJ
GILLETT GT
TAGGART RT
THAKKER RV
Citation: Jt. Pang et al., GENETIC-MAPPING STUDIES OF 40 LOCI AND 23 COSMIDS IN CHROMOSOME-11P13-11Q13, AND EXCLUSION OF MU-CALPAIN AS THE MULTIPLE ENDOCRINE NEOPLASIA TYPE-1 GENE, Human genetics, 97(6), 1996, pp. 732-741
Authors:
LLOYD SE
PEARCE SHS
FISHER SE
STEINMEYER K
SCHWAPPACH B
SCHEINMAN SJ
HARDING B
BOLINO A
DEVOTO M
GOODYER P
RIGDEN SPA
WRONG O
JENTSCH TJ
CRAIG IW
THAKKER RV
Citation: Se. Lloyd et al., A COMMON MOLECULAR-BASIS FOR 3 INHERITED KIDNEY-STONE DISEASES, Nature, 379(6564), 1996, pp. 445-449
Citation: B. Harding, LAMINAR HETEROTOPIA - A POSSIBLE FAILURE OF PROGRAMMED CELL-DEATH, Journal of neuropathology and experimental neurology, 55(5), 1996, pp. 21-21
Authors:
LLOYD SE
PEARCE SIS
FISHER SE
HARDING B
SCHEINMAN SJ
GOODYER P
WRONG OM
CRAIG IW
THAKKER RV
Citation: Se. Lloyd et al., HEREDITARY NEPHROLITHIASIS IS ASSOCIATED WITH MUTATIONS IN AN X-LINKED CHLORIDE CHANNEL GENE, Journal of bone and mineral research, 10, 1995, pp. 175-175
Citation: B. Harding et al., A CASE OF PELIZAEUS-MERZBACHER DISEASE SHOWING INCREASED DOSAGE OF THE PROTEOLIPID PROTEIN GENE, Neuropathology and applied neurobiology, 21(2), 1995, pp. 111-115
Citation: B. Harding, PHOTO PORTFOLIO, THE FLAHERTY IN ACTION + A SELECTION OF CANDID SHOTSOF THE PARTICIPANTS FROM THE SEMINARS OVER THE PAST 30 YEARS, Wide angle, 17(1-4), 1995, pp. 81
Citation: B. Harding et E. Barnouw, PORTRAIT GALLERY + A SELECTION OF PHOTOGRAPHS AND EDITED EXCERPTS FROM INTERVIEWS WITH PEOPLE WHO HAD WORKED WITH FLAHERTY,ROBERT, Wide angle, 17(1-4), 1995, pp. 345-366