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Results: 1-25/30
Authors:
MARSH DJ
COULON V
LUNETTA KL
ROCCASERRA P
DAHIA PLM
ZHENG ZM
LIAW D
CARON S
DUBOUE B
LIN AY
RICHARDSON AL
BONNETBLANC JM
BRESSIEUX JM
CABARROTMOREAU A
CHOMPRET A
DEMANGE L
EELES RA
YAHANDA AM
FEARON ER
FRICKER JP
GORLIN RJ
HODGSON SV
HUSON S
LACOMBE D
LEPRAT F
ODENT S
TOULOUSE C
OLOPADE OI
SOBOL H
TISHLER S
WOODS CG
ROBINSON BG
WEBER HC
PARSONS R
PEACOCKE M
LONGY M
ENG C
Citation: Dj. Marsh et al., MUTATION SPECTRUM AND GENOTYPE-PHENOTYPE ANALYSES IN COWDEN-DISEASE AND BANNAYAN-ZONANA-SYNDROME, 2 HAMARTOMA SYNDROMES WITH GERMLINE PTEN MUTATION, Human molecular genetics, 7(3), 1998, pp. 507-515
Authors:
GARDNER RJM
WOODS CG
Citation: Rjm. Gardner et Cg. Woods, A SYNDROME OF A DISTINCTIVE FACIES AND NORMAL NEUROLOGY, Clinical dysmorphology, 7(2), 1998, pp. 155-156
Authors:
WEBB T
CLARKE A
HANEFELD F
PEREIRA JL
ROSENBLOOM L
WOODS CG
Citation: T. Webb et al., LINKAGE ANALYSIS IN RETT-SYNDROME FAMILIES SUGGESTS THAT THERE MAY BEA CRITICAL REGION AT XQ28, Journal of Medical Genetics, 35(12), 1998, pp. 997-1003
Authors:
NAZEM E
BISHOP DT
QUIRKE P
WOODS CG
Citation: E. Nazem et al., TUMOR-SUPPRESSOR GENES VERSUS POLY-A TRACT MARKERS IN THE DETECTION OF MICROSATELLITE INSTABILITY IN COLORECTAL-CANCER, British Journal of Cancer, 78, 1998, pp. 154-154
Authors:
WOODS CG
Citation: Cg. Woods, DNA-REPAIR DISORDERS, Archives of Disease in Childhood, 78(2), 1998, pp. 178-184
Authors:
JACKSON AP
MCHALE DP
CAMPBELL DA
JAFRI H
RASHID Y
MANNAN J
KARBANI G
CORRY P
LEVENE MI
MUELLER RF
MARKHAM AF
LENCH NJ
WOODS CG
Citation: Ap. Jackson et al., PRIMARY AUTOSOMAL RECESSIVE MICROCEPHALY (MCPH1) MAPS TO CHROMOSOME 8P22-PTER, American journal of human genetics, 63(2), 1998, pp. 541-546
Authors:
ROBERTS E
DEEBLE VJ
WOODS CG
TAYLOR GR
Citation: E. Roberts et al., POTASSIUM-PERMANGANATE AND TETRAETHYLAMMONIUM CHLORIDE ARE A SAFE ANDEFFECTIVE SUBSTITUTE FOR OSMIUM-TETROXIDE IN SOLID-PHASE FLUORESCENT CHEMICAL CLEAVAGE OF MISMATCH, Nucleic acids research, 25(16), 1997, pp. 3377-3378
Authors:
TRENT RJ
SHEFFIELD LJ
DENG ZM
KIM WS
NASSIF NT
RYCE C
WOODS CG
MICHAELIS RC
TARLETON J
SMITH A
Citation: Rj. Trent et al., THE ELUSIVE ANGELMAN-SYNDROME CRITICAL REGION, Journal of Medical Genetics, 34(9), 1997, pp. 714-718
Authors:
WOODS CG
NOBLE J
FALCONER AR
Citation: Cg. Woods et al., A STUDY OF BROTHERS WITH KLINEFELTER-SYNDROME, Journal of Medical Genetics, 34(8), 1997, pp. 702-702
Authors:
NAZEM E
WOODS CG
TAYLOR GR
QUIRKE P
BISHOP T
Citation: E. Nazem et al., INSTABILITY OF POLY-A TRACTS IN SPORADIC BOWEL CANCERS, Journal of Medical Genetics, 34, 1997, pp. 209-209
Authors:
ROWLAND JS
WOODS CG
TAYLOR GR
Citation: Js. Rowland et al., X-INACTIVATION STUDIES USING METHYLATION SENSITIVE AND METHYLATION DEPENDENT ENZYME SITES NEAR THE POLYMORPHIC CAG REPEAT IN THE HUMAN ANDROGEN RECEPTOR GENE - A MIRROR-IMAGE, Journal of Medical Genetics, 34, 1997, pp. 1305-1305
Authors:
DEEBLE J
WHITEHOUSE A
MEREDITH DM
MARKHAM AF
WOODS CG
TAYLOR GR
Citation: J. Deeble et al., USE OF THERMUS-THERMOPHILUS HB8 MUTS IN A FILTER BINDING FORMAT FOR MISMATCH DETECTION, Journal of Medical Genetics, 34, 1997, pp. 1306-1306
Authors:
ROBERTS E
DEEBLE VJ
WOODS CG
BISHOP DT
TAYLOR GR
Citation: E. Roberts et al., COMPARISON OF ENZYME MISMATCH CLEAVAGE AND CHEMICAL CLEAVAGE OF MISMATCH ON A DEFINED SET OF HETERODUPLEXES, Journal of Medical Genetics, 34, 1997, pp. 1406-1406
Authors:
WOODS CG
ROBINSON M
GARDINER C
ROUSSOUNIS T
Citation: Cg. Woods et al., 4 CASES OF THE CONDITION DESCRIBED BY BUNDEY WITH AUTISM AND A MATERNAL 15Q11-13 DUPLICATION, American journal of human genetics, 61(4), 1997, pp. 658-658
Authors:
DEEBLE JV
WHITEHOUSE A
ROBERTS E
WOODS CG
MEREDITH D
MARKHAM AF
TAYLOR GR
Citation: Jv. Deeble et al., EVALUATION OF ENZYMATIC METHODS OF MUTATION DETECTION, American journal of human genetics, 61(4), 1997, pp. 1266-1266
Authors:
ROBERTS E
DEEBLE JV
ROBINSON MD
WOODS CG
BISHOP DT
TAYLOR GR
Citation: E. Roberts et al., DEVELOPMENTS IN CHEMICAL CLEAVAGE OF MISMATCH AND DETECTION OF BRCA1 AND BRCA2 MUTATIONS BY PERMANGANATE-MEDIATED MISMATCH CLEAVAGE, American journal of human genetics, 61(4), 1997, pp. 1313-1313
Authors:
MORISON IM
BECROFT DM
TANIGUCHI T
WOODS CG
REEVE AE
Citation: Im. Morison et al., SOMATIC OVERGROWTH ASSOCIATED WITH OVEREXPRESSION OF INSULIN-LIKE GROWTH-FACTOR-II, Nature medicine, 2(3), 1996, pp. 311-316
Authors:
CARR AJ
SMITH R
ATHANASOU N
WOODS CG
Citation: Aj. Carr et al., FIBROGENESIS IMPERFECTA OSSIUM, Journal of bone and joint surgery. British volume, 77(5), 1995, pp. 820-829
Authors:
QIN WN
WOODS CG
SCHNEIDER JA
WOODS WT
Citation: Wn. Qin et al., ORGANIZATION AND FINE-STRUCTURE OF A PACEMAKER DERIVED FROM FETAL-RATMYOCARDIUM, Pediatric research, 37(3), 1995, pp. 283-288
Authors:
WOODS CG
LEVERSHA M
ROGERS JG
Citation: Cg. Woods et al., SEVERE INTRAUTERINE GROWTH-RETARDATION WITH INCREASED MITOMYCIN-C SENSITIVITY - A FURTHER CHROMOSOME BREAKAGE SYNDROME, Journal of Medical Genetics, 32(4), 1995, pp. 301-305
Authors:
SCHULZE LJH
WOODS CG
Citation: Ljh. Schulze et Cg. Woods, EFFECTIVENESS OF WORKPLACE ACCOMMODATIONS FOR A CORPORATE TELEPHONE OPERATOR WITH A FULL LEFT-ARM PROSTHESIS - A CASE-STUDY, Journal of occupational rehabilitation, 4(2), 1994, pp. 77-86
Authors:
QIN WN
WOODS CG
SCHNEIDER JA
WOODS WT
Citation: Wn. Qin et al., DIFFERENTIATION OF CELLS WITH CONDUCTION SYSTEM PHENOTYPE FROM FETAL VENTRICULAR MYOCYTES, Journal of the American College of Cardiology, 1994, pp. 10000330-10000330
Authors:
WOODS CG
BANKIER A
CURRY J
SHEFFIELD LJ
SLANEY SF
SMITH K
VOULLAIRE L
WELLESLEY D
Citation: Cg. Woods et al., ASYMMETRY AND SKIN PIGMENTARY ANOMALIES IN CHROMOSOME MOSAICISM, Journal of Medical Genetics, 31(9), 1994, pp. 694-701
Authors:
WOODS CG
SHEFFIELD LJ
Citation: Cg. Woods et Lj. Sheffield, FURTHER FAMILY WITH AUTOSOMAL-DOMINANT PATENT DUCTUS-ARTERIOSUS, Journal of Medical Genetics, 31(8), 1994, pp. 659-659
Authors:
WOODS CG
ROGERS JG
MAYNE V
Citation: Cg. Woods et al., 2 SIBS WHO ARE DOUBLE HETEROZYGOTES FOR ACHONDROPLASIA AND PSEUDOACHONDROPLASTIC DYSPLASIA, Journal of Medical Genetics, 31(7), 1994, pp. 565-569