AAAAAA
Results: 1-25/33
Authors:
MICHAELIS RC
VELAGALETI GVN
JONES C
PIVNICK EK
PHELAN MC
BOYD E
TARLETON J
WILROY RS
TUNNACLIFFE A
THARAPEL AT
Citation: Rc. Michaelis et al., MOST JACOBSEN-SYNDROME DELETION BREAKPOINTS OCCUR DISTAL TO FRA11B, American journal of medical genetics, 76(3), 1998, pp. 222-228
Authors:
GHAFFARI SR
BOYD E
TOLMIE JL
CROW YJ
TRAINER AH
CONNER JM
Citation: Sr. Ghaffari et al., A NEW STRATEGY FOR CRYPTIC TELOMERIC TRANSLOCATION SCREENING IN PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION, Journal of Medical Genetics, 35(3), 1998, pp. 225-233
Authors:
GHAFFARI SR
BOYD E
CONNOR JM
JONES AM
TOLMIE JL
Citation: Sr. Ghaffari et al., MOSAIC SUPERNUMERARY RING CHROMOSOME-19 IDENTIFIED BY COMPARATIVE GENOMIC HYBRIDIZATION, Journal of Medical Genetics, 35(10), 1998, pp. 836-840
Authors:
BOYD E
Citation: E. Boyd, AIDS COUNSELING - INSTITUTIONAL INTERACTION AND CLINICAL-PRACTICE - PERAKYLA,A, Discourse & society, 8(3), 1997, pp. 420-423
Authors:
LOWTHER GW
MORRIS A
DHANJAL S
YOUNG J
MENZIES A
BOYD E
CONNOR JM
Citation: Gw. Lowther et al., THE INTRODUCTION OF A RAPID, DIAGNOSTIC, PRENATAL TEST FOR DOWNS-SYNDROME USING FISH ON UNCULTURED AMNIOCYTES, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 76-76
Authors:
MORRISON N
TOLMIE J
DUNLOP A
DAVIDSON N
JAMIESON A
BREWER C
BOYD E
Citation: N. Morrison et al., CHROMOSOME 22Q11.2 MICRODELETION - WHAT ARE THE DIFFERENTIAL DIAGNOSES, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 256-256
Authors:
ACAR H
STEWART J
BOYD E
CONNER MJ
Citation: H. Acar et al., IDENTIFICATION OF VARIANT TRANSLOCATIONS IN CHRONIC MYELOID-LEUKEMIA BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cancer genetics and cytogenetics, 93(2), 1997, pp. 115-118
Authors:
GHAFFARI SR
BOYD E
CROW Y
TRAINER AH
TOLMIE J
CONNOR JM
Citation: Sr. Ghaffari et al., A NOVEL STRATEGY FOR CRYPTIC TELOMERIC TRANSLOCATION SCREENING IN PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION, Journal of Medical Genetics, 34, 1997, pp. 65-65
Authors:
GHAFFARI SR
BOYD E
STEWART J
CONNOR JM
Citation: Sr. Ghaffari et al., COMPARATIVE GENOMIC HYBRIDIZATION IN THE INVESTIGATION OF HEMATOLOGICAL MALIGNANCIES, Journal of Medical Genetics, 34, 1997, pp. 232-232
Authors:
MONADDES SM
BOYD E
CONNOR JM
Citation: Sm. Monaddes et al., COMPARISON OF A CHROMOSOME-13 SPECIFIC COSMID CONTIG AND AN ALU-PCR AMPLIFIED YAC PROBES DEVELOPED TO DETECT THE COPY NUMBER OF CHROMOSOME-13 ON UNCULTURED LYMPHOCYTES AND AMNIOCYTES BY FISH, Journal of Medical Genetics, 34, 1997, pp. 1202-1202
Authors:
GHAFFARI SR
BOYD E
TOLMIE JL
CONNOR JM
Citation: Sr. Ghaffari et al., COMPARATIVE GENOMIC HYBRIDIZATION REVEALS THE ORIGIN OF A MOSAIC, SUPERNUMERARY RING CHROMOSOME-19 IN A 70-YEAR-OLD LADY WITH MENTAL-RETARDATION, Journal of Medical Genetics, 34, 1997, pp. 1207-1207
Authors:
MONADDES SM
BOYD E
CONNOR JM
Citation: Sm. Monaddes et al., COMPARISON OF A CHROMOSOME-13 SPECIFIC COSMID CONTIG AND AN ALU-PCR AMPLIFIED YAC PROBES DEVELOPED TO DETECT THE COPY NUMBER OF CHROMOSOME-13 ON UNCULTURED LYMPHOCYTES AND AMNIOCYTES BY FISH, Journal of Medical Genetics, 34, 1997, pp. 1212-1212
Authors:
SEAVER LH
BOYD E
Citation: Lh. Seaver et E. Boyd, SPONDYLOCARPOTARSAL SYNOSTOSIS SYNDROME IN A 5-YEAR-OLD GIRL AND REVIEW OF 12 CASES, American journal of human genetics, 61(4), 1997, pp. 633-633
Authors:
LOWTHER GW
MORRIS A
YOUNG J
MENZIES A
WATT J
BOYD E
CONNOR JM
Citation: Gw. Lowther et al., DOWNS-SYNDROME DETECTION ON UNCULTURED AMNIOCYTES USING FISH - ONE YEARS DIAGNOSTIC EXPERIENCE, American journal of human genetics, 61(4), 1997, pp. 904-904
Authors:
MOHADDES SM
BOYD E
MORRIS A
MORRISON N
CONNOR JM
Citation: Sm. Mohaddes et al., A PRACTICAL STRATEGY FOR DETECTION OF MAJOR CHROMOSOME ANEUPLOIDIES USING RATIO-MIXING FLUORESCENCE IN-SITU HYBRIDIZATION, Molecular and cellular probes, 10(2), 1996, pp. 147-154
Authors:
BOYD E
Citation: E. Boyd, PERSISTANCE PAYS + RESPONSE TO COHEN,JONATHAN AND CREWS,FREDERICK ARTICLES ON SCIENTIFIC VERIFICATION OF TRUTH, The American book review, 17(5), 1996, pp. 3-3
Authors:
REID E
MORRISON N
BARREN L
BOYD E
COOKE A
FIELDING D
TOLMIE JL
Citation: E. Reid et al., FAMILIAL WOLF-HIRSCHHORN SYNDROME RESULTING FROM A CRYPTIC TRANSLOCATION - A CLINICAL AND MOLECULAR STUDY, Journal of Medical Genetics, 33(3), 1996, pp. 197-202
Authors:
BARNICOAT AJ
BONNEAU JL
BOYD E
DOCHERTY Z
FENNELL SJ
HURET JL
KING M
MALTBY EL
MCMANUS S
PILZ DT
SHAFEIBENAISSA E
SUPER M
TOLMIE J
Citation: Aj. Barnicoat et al., DOWN-SYNDROME WITH PARTIAL DUPLICATION AND DEL(21) SYNDROME - STUDY PROTOCOL AND CALL FOR COLLABORATION - STUDY-I - CLINICAL-ASSESSMENT, Clinical genetics, 49(1), 1996, pp. 20-27
Authors:
HUGHES B
HOWAT D
LISLE H
HOLBROOK M
JAMES T
GOZZARD N
BLEASE K
HUGHES P
KINGABY R
WARRELLOW G
ALEXANDER R
HEAD J
BOYD E
EATON M
PERRY M
WALES M
SMITH B
OWENS R
CATTERALL C
LUMB S
RUSSELL A
ALLEN R
MERRIMAN M
BLOXHAM D
HIGGS G
Citation: B. Hughes et al., THE INHIBITION OF ANTIGEN-INDUCED EOSINOPHILIA AND BRONCHOCONSTRICTION BY CDP840, A NOVEL STEREOSELECTIVE INHIBITOR OF PHOSPHODIESTERASE TYPE-4, British Journal of Pharmacology, 118(5), 1996, pp. 1183-1191
Authors:
MCBRIDE MW
RUSSELL AJ
VASS K
FRANKRAUE K
CRAIG NJ
MORRISON N
BOYD E
SZPIRER C
SUTCLIFFE RG
Citation: Mw. Mcbride et al., THE HUMAN 3-BETA-HYDROXYSTEROID DEHYDROGENASE (3-BETA-HSD) GENE-CLUSTER ON CHROMOSOME 1P13 CONTAINS A PRESUMPTIVE PSEUDOGENE - 3-BETA-HSD AND CYP17 DO NOT SEGREGATE WITH DOMINANTLY INHERITED HIRSUTISM, Journal of molecular endocrinology, 15(2), 1995, pp. 167-176
Authors:
MCBRIDE MW
RUSSELL AJ
VASS K
FORSTER V
BURRIDGE SM
MORRISON N
BOYD E
PONDER BAJ
SUTCLIFFE RG
Citation: Mw. Mcbride et al., NEW MEMBERS OF THE 3-BETA-HYDROXYSTEROID DEHYDROGENASE GENE FAMILY, Molecular and cellular probes, 9(2), 1995, pp. 121-128
Authors:
CHU CE
DONALDSON MDC
KELNAR C
SMAIL P
GREENE S
BOYD E
CONNOR JM
Citation: Ce. Chu et al., X-INACTIVATION STUDIES IN PATIENTS WITH TURNERS-SYNDROME AND RING X-CHROMOSOMES, Journal of Medical Genetics, 32(2), 1995, pp. 153-153
Authors:
STAMATAKOS MD
HOUSTON GD
FOWLER CB
BOYD E
SOLANKI PH
Citation: Md. Stamatakos et al., DIAGNOSIS OF AMELOBLASTOMA OF THE MAXILLA BY FINE-NEEDLE ASPIRATION -A CASE-REPORT, Acta cytologica, 39(4), 1995, pp. 817-820
Authors:
MARINONI JC
BOYD E
SHERMAN S
SCHWARTZ C
Citation: Jc. Marinoni et al., FAMILIAL SPLIT HAND SPLIT FOOT LONG-BONE DEFICIENCY DOES NOT SEGREGATE WITH MARKERS LINKED TO THE SHFD1 LOCUS IN 7Q21.3-Q22.1, Human molecular genetics, 3(8), 1994, pp. 1355-1357
Authors:
KEANE D
BOYD E
ANDERSON D
ROBLES A
DEVERALL P
MORRIS R
JACKSON G
SOWTON E
Citation: D. Keane et al., COMPARISON OF BIPHASIC AND MONOPHASIC WAVE-FORMS IN EPICARDIAL ATRIALDEFIBRILLATION, Journal of the American College of Cardiology, 24(1), 1994, pp. 171-176