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Results: 1-25 | 26-50 | 51-60
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ISOLATION OF A CDNA-DERIVED EXPRESSED-SEQUENCE-TAG CLONE ON CHROMOSOME-15
Authors: KIM WS SMITH A TRENT RJ
Citation: Ws. Kim et al., ISOLATION OF A CDNA-DERIVED EXPRESSED-SEQUENCE-TAG CLONE ON CHROMOSOME-15, Disease markers, 12(4), 1996, pp. 275-278
COINHERITANCE OF OTHER CHROMOSOME-15 ABNORMALITIES WITH PRADER-WILLI-SYNDROME - GENETIC RISK-ESTIMATION AND MAPPING
Authors: ROGAN PK MASCARI MJ LADDA RL WOODAGE T TRENT RJ SMITH A LAI LW ERICKSON RP CASSIDY SB PETERSEN MB MIKKELSEN M DRISCOLL DJ NICHOLLS RD BUTLER MG
Citation: Pk. Rogan et al., COINHERITANCE OF OTHER CHROMOSOME-15 ABNORMALITIES WITH PRADER-WILLI-SYNDROME - GENETIC RISK-ESTIMATION AND MAPPING, American journal of medical genetics, 62(3), 1996, pp. 6-6
A VARIABLE THRESHOLD EDGE-DETECTOR FOR IMPROVED QUANTITATION OF GATEDTOMOGRAPHIC IMAGING OF THE LEFT-VENTRICULAR BLOOD-POOL
Authors: MCKIDDIE FI GEMMELL HG REDPATH TW TRENT RJ PHILIP WJU NORTON MY SMITH FW
Citation: Fi. Mckiddie et al., A VARIABLE THRESHOLD EDGE-DETECTOR FOR IMPROVED QUANTITATION OF GATEDTOMOGRAPHIC IMAGING OF THE LEFT-VENTRICULAR BLOOD-POOL, Nuclear medicine communications, 17(5), 1996, pp. 410-417
CLINICAL-FEATURES IN 27 PATIENTS WITH ANGELMAN SYNDROME RESULTING FROM DNA DELETION
Authors: SMITH A WILES C HAAN E MCGILL J WALLACE G DIXON J SELBY R COLLEY A MARKS R TRENT RJ
Citation: A. Smith et al., CLINICAL-FEATURES IN 27 PATIENTS WITH ANGELMAN SYNDROME RESULTING FROM DNA DELETION, Journal of Medical Genetics, 33(2), 1996, pp. 107-112
DNA TESTING IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - CLINICAL AND LABORATORY IMPLICATIONS
Authors: SMART RV YU B LE H FRENCH JA RICHMOND DR JEREMY RW SEMSARIAN C CHEUNG L ROSS DA TRENT RJ
Citation: Rv. Smart et al., DNA TESTING IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - CLINICAL AND LABORATORY IMPLICATIONS, Clinical genetics, 50(4), 1996, pp. 169-175
THE RISKS OF THROMBOLYSIS IN PATIENTS WITHOUT ACUTE MYOCARDIAL-INFARCTION
Authors: ADAMS JN JAMIESON M TRENT RJ RAWLES J JENNINGS KP
Citation: Jn. Adams et al., THE RISKS OF THROMBOLYSIS IN PATIENTS WITHOUT ACUTE MYOCARDIAL-INFARCTION, International journal of cardiology, 51(2), 1995, pp. 177-181
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY AND THE NEW GENETICS
Authors: RICHMOND DR JEREMY RW TRENT RJ
Citation: Dr. Richmond et al., FAMILIAL HYPERTROPHIC CARDIOMYOPATHY AND THE NEW GENETICS, Medical journal of Australia, 162(2), 1995, pp. 62-63
MARFANS-SYNDROME - AORTIC DISTENSIBILITY (MEASURED BY MRI) AND FAMILYPHENOTYPE
Authors: DEAN JCS ADAMS JN BROOKES M GRAY JR REDPATH TW SMITH FW WALTON S TRENT RJ
Citation: Jcs. Dean et al., MARFANS-SYNDROME - AORTIC DISTENSIBILITY (MEASURED BY MRI) AND FAMILYPHENOTYPE, Journal of Medical Genetics, 32(2), 1995, pp. 149-149
CYSTIC-FIBROSIS HETEROZYGOSITY AND ALCOHOLIC PANCREATITIS
Authors: NORTON ID APTE MV DIXSON H TRENT RJ PIROLA RC WILSON JS
Citation: Id. Norton et al., CYSTIC-FIBROSIS HETEROZYGOSITY AND ALCOHOLIC PANCREATITIS, Gastroenterology, 108(4), 1995, pp. 380-380
AORTIC DISTENSIBILITY AND STIFFNESS INDEX MEASURED BY MAGNETIC-RESONANCE-IMAGING IN PATIENTS WITH MARFANS-SYNDROME
Authors: ADAMS JN BROOKS M REDPATH TW SMITH FW DEAN J GRAY J WALTON S TRENT RJ
Citation: Jn. Adams et al., AORTIC DISTENSIBILITY AND STIFFNESS INDEX MEASURED BY MAGNETIC-RESONANCE-IMAGING IN PATIENTS WITH MARFANS-SYNDROME, British Heart Journal, 73(3), 1995, pp. 265-269
DELAY BETWEEN THE ONSET OF SYMPTOMS OF ACUTE MYOCARDIAL-INFARCTION AND SEEKING MEDICAL ASSISTANCE IS INFLUENCED BY LEFT-VENTRICULAR FUNCTION AT PRESENTATION
Authors: TRENT RJ ROSE EL ADAMS JN JENNINGS KP RAWLES JM
Citation: Rj. Trent et al., DELAY BETWEEN THE ONSET OF SYMPTOMS OF ACUTE MYOCARDIAL-INFARCTION AND SEEKING MEDICAL ASSISTANCE IS INFLUENCED BY LEFT-VENTRICULAR FUNCTION AT PRESENTATION, British Heart Journal, 73(2), 1995, pp. 125-128
WOMEN AND MYOCARDIAL-INFARCTION - AGISM RATHER THAN SEXISM
Authors: ADAMS JN JAMIESON M RAWLES JM TRENT RJ JENNINGS KP
Citation: Jn. Adams et al., WOMEN AND MYOCARDIAL-INFARCTION - AGISM RATHER THAN SEXISM, British Heart Journal, 73(1), 1995, pp. 87-91
COMPARISON OF HIGH-RESOLUTION CYTOGENETICS, FLUORESCENCE IN-SITU HYBRIDIZATION, AND DNA STUDIES TO VALIDATE THE DIAGNOSIS OF PRADER-WILLI AND ANGELMANS SYNDROMES
Authors: SMITH A PRASAD M DENG ZM ROBSON L WOODAGE T TRENT RJ
Citation: A. Smith et al., COMPARISON OF HIGH-RESOLUTION CYTOGENETICS, FLUORESCENCE IN-SITU HYBRIDIZATION, AND DNA STUDIES TO VALIDATE THE DIAGNOSIS OF PRADER-WILLI AND ANGELMANS SYNDROMES, Archives of Disease in Childhood, 72(5), 1995, pp. 397-402
A PHYSICAL MAP OF THE ANGELMAN SYNDROME CRITICAL REGION AT LOCUS D15S113 (LS6-1)
Authors: TRENT RJ NASSIF N DENG ZM KIM S PRASAD M SMITH A ROSS DA
Citation: Rj. Trent et al., A PHYSICAL MAP OF THE ANGELMAN SYNDROME CRITICAL REGION AT LOCUS D15S113 (LS6-1), American journal of human genetics, 57(4), 1995, pp. 1580-1580
EXON-8 APC MUTATIONS ACCOUNT FOR A DISPROPORTIONATE NUMBER OF FAMILIAL ADENOMATOUS POLYPOSIS FAMILIES
Authors: KOOREY DJ MCCAUGHAN GW TRENT RJ GALLAGHER ND
Citation: Dj. Koorey et al., EXON-8 APC MUTATIONS ACCOUNT FOR A DISPROPORTIONATE NUMBER OF FAMILIAL ADENOMATOUS POLYPOSIS FAMILIES, Human mutation, 3(1), 1994, pp. 12-18
PHYSICAL MAPPING STUDIES AT D15S10 - IMPLICATIONS FOR CANDIDATE GENE IDENTIFICATION IN THE ANGELMAN SYNDROME PRADER-WILLI SYNDROME CHROMOSOME REGION OF 15Q11-Q13/
Authors: WOODAGE T LINDEMAN R DENG ZM FIMMEL A SMITH A TRENT RJ
Citation: T. Woodage et al., PHYSICAL MAPPING STUDIES AT D15S10 - IMPLICATIONS FOR CANDIDATE GENE IDENTIFICATION IN THE ANGELMAN SYNDROME PRADER-WILLI SYNDROME CHROMOSOME REGION OF 15Q11-Q13/, Genomics, 19(1), 1994, pp. 170-172
A 3.5 KB DELETION IN THE GLYCOPHORIN-C GENE ACCOUNTS FOR THE GERBICH-NEGATIVE BLOOD-GROUP IN MELANESIANS
Authors: SERJEANTSON SW WHITE BS BHATIA K TRENT RJ
Citation: Sw. Serjeantson et al., A 3.5 KB DELETION IN THE GLYCOPHORIN-C GENE ACCOUNTS FOR THE GERBICH-NEGATIVE BLOOD-GROUP IN MELANESIANS, Immunology and cell biology, 72(1), 1994, pp. 23-27
FAMILIAL UNBALANCED TRANSLOCATION T(8 15)(P23.3 Q11) WITH UNIPARENTALDISOMY IN ANGELMAN SYNDROME
Authors: SMITH A DENG ZM BERAN R WOODAGE T TRENT RJ
Citation: A. Smith et al., FAMILIAL UNBALANCED TRANSLOCATION T(8 15)(P23.3 Q11) WITH UNIPARENTALDISOMY IN ANGELMAN SYNDROME, Human genetics, 93(4), 1994, pp. 471-473
PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY
Authors: ROGAN PK MASCARI MJ LADDA RL WOODAGE T TRENT RJ SMITH A LAI LW ERICKSON RP CASSIDY SB PETERSEN MB MIKKELSEN M DRISCOLL DJ NICHOLLS RD
Citation: Pk. Rogan et al., PERTURBED RECOMBINATION OF CHROMOSOME-15 IN PRADER-WILLI PATIENTS WITH MATERNAL DISOMY, Cytogenetics and cell genetics, 67(1), 1994, pp. 18-18
CONSTRUCTION AND CHARACTERIZATION OF LAMBDA-PHAGE CONTIGS OF YACS MAPPING TO 15Q11-]Q13
Authors: DENG ZM KIM WS NASSIF NT WOODAGE T SMITH A TRENT RJ
Citation: Zm. Deng et al., CONSTRUCTION AND CHARACTERIZATION OF LAMBDA-PHAGE CONTIGS OF YACS MAPPING TO 15Q11-]Q13, Cytogenetics and cell genetics, 67(1), 1994, pp. 20-20
LOCALIZATION OF THE BLOOM-SYNDROME GONE BY HOMOZYGOSITY MAPPING IN A PATIENT WITH MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME-15
Authors: WOODAGE T PRASAD M DIXON JW SELBY RE ROMAIN DR COLUMBANOGREEN LM GRAHAM D SEIP JR ROGAN PK SMITH A TRENT RJ
Citation: T. Woodage et al., LOCALIZATION OF THE BLOOM-SYNDROME GONE BY HOMOZYGOSITY MAPPING IN A PATIENT WITH MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME-15, Cytogenetics and cell genetics, 67(1), 1994, pp. 21-21
AN ANALYSIS OF 900 CONSECUTIVE ADMISSIONS TO A REGIONAL INFECTION UNIT
Authors: DYKHUIZEN RS TRENT RJ PACITTI DP REID TM DOUGLAS JG SMITH CC
Citation: Rs. Dykhuizen et al., AN ANALYSIS OF 900 CONSECUTIVE ADMISSIONS TO A REGIONAL INFECTION UNIT, The Journal of infection, 29(2), 1994, pp. 189-193
A VARIETY OF GENETIC MECHANISMS ARE ASSOCIATED WITH THE PRADER-WILLI-SYNDROME
Authors: WOODAGE T DENG ZM PRASAD M SMART R LINDEMAN R CHRISTIAN SL LEDBETTER DH ROBSON L SMITH A TRENT RJ
Citation: T. Woodage et al., A VARIETY OF GENETIC MECHANISMS ARE ASSOCIATED WITH THE PRADER-WILLI-SYNDROME, American journal of medical genetics, 54(3), 1994, pp. 219-226
THE AUSTRALIAN TYPE OF NONDELETIONAL (G)GAMMA-HPFH HAS A C-]G SUBSTITUTION AT NUCLEOTIDE-114 OF THE (G)GAMMA GENE
Authors: MOTUM PI DENG ZM HUONG L TRENT RJ
Citation: Pi. Motum et al., THE AUSTRALIAN TYPE OF NONDELETIONAL (G)GAMMA-HPFH HAS A C-]G SUBSTITUTION AT NUCLEOTIDE-114 OF THE (G)GAMMA GENE, British Journal of Haematology, 86(1), 1994, pp. 219-221
BLOOM-SYNDROME AND MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-15
Authors: WOODAGE T PRASAD M DIXON JW SELBY RE ROMAIN DR COLUMBANOGREEN LM GRAHAM D ROGAN PK SEIP JR SMITH A TRENT RJ
Citation: T. Woodage et al., BLOOM-SYNDROME AND MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME-15, American journal of human genetics, 55(1), 1994, pp. 74-80
Risultati: 1-25 | 26-50 | 51-60