Search Results - "Lawler, S. D"

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    A prospective genetic study of complete and partial hydatidiform moles by Lawler, S D, Fisher, R A, Dent, J

    “…Two hundred two hydatidiform moles were classified by pathologic features and ploidy into partial or complete moles. Further classification was made by using…”
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    A novel abl protein expressed in Philadelphia chromosome positive acute lymphoblastic leukaemia by CHAN, L. C, KARHI, K. K, WIEDEMANN, L. M, RAYTER, S. I, HEISTERKAMP, N, ERIDANI, S, POWLES, R, LAWLER, S. D, GROFFEN, J, FOULKES, J. G, GREAVES, M. F

    Published in Nature (London) (12-02-1987)
    “…The Philadelphia (Ph) chromosome breakpoints in chronic myelocytic leukaemia are clustered on chromosome 22 band q11 in a 5.8-kilobase (kb) region designated…”
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    Gestational trophoblastic tumours following initial diagnosis of partial hydatidiform mole by Bagshawe, K D, Lawler, S D, Paradinas, F J, Dent, J, Brown, P, Boxer, G M

    Published in The Lancet (British edition) (05-05-1990)
    “…11 patients registered with an initial diagnosis of partial hydatidiform mole (PHM) subsequently required chemotherapy for a gestational trophoblastic tumour…”
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    Genetically homozygous choriocarcinoma following pregnancy with hydatidiform mole by FISHER, R. A, LAWLER, S. D, POVEY, S, BAGSHAWE, K. D

    Published in British journal of cancer (01-12-1988)
    “…Genetic studies have been made in two cases of primary choriocarcinoma from patients in whom the antecedent pregnancy was a hydatidiform mole. Restriction…”
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    Genetic studies in hydatidiform mole with clinical correlations by Lawler, S D, Fisher, R A

    Published in Placenta (Eastbourne) (01-01-1987)
    “…In an elective study of 163 hydatidiform moles 38 were classified as partial mole (PHM) and 125 as complete mole (CHM) on the basis of pathology. Genetic…”
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    Frequency of heterozygous complete hydatidiform moles, estimated by locus-specific minisatellite and Y chromosome-specific probes by FISHER, R. A, POVEY, S, JEFFREYS, A. J, MARTIN, C. A, PATEL, I, LAWLER, S. D

    Published in Human genetics (01-06-1989)
    “…Restriction fragment length polymorphisms identified with three locus-specific minisatellite probes and banding patterns with Y chromosome-specific probes have…”
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  8. 8

    A myeloproliferative disease in two infants associated with eosinophilia and chromosome t(1;5) translocation by Darbyshire, P J, Shortland, D, Swansbury, G J, Sadler, J, Lawler, S D, Chessells, J M

    Published in British journal of haematology (01-08-1987)
    “…Two children are described who presented at the age of 5 and 7 months with anaemia, a high white cell count with eosinophilia and thrombocytopenia. Both…”
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    ABO genotyping of complete hydatidiform moles by Fisher, R A, Johnson, P H, Povey, S, Hopkinson, D A, Lawler, S D

    Published in Disease markers (01-11-1993)
    “…It has been suggested that the ABO blood group of a patient and her partner influence the clinical outcome for patients having a pregnancy with a complete…”
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  10. 10

    Cytogenetic studies on recipients of allogeneic bone marrow using the sex chromosomes as markers of cellular origin by Lawler, S D, Baker, M C, Harris, H, Morgenstern, G R

    Published in British journal of haematology (01-03-1984)
    “…In 45 patients whose donor was of unlike sex, the sex chromosomes were used as markers of the cellular origin of myeloid and lymphoid tissues after allogeneic…”
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    Genetic studies on hydatidiform moles. II. The origin of complete moles by Lawler, S D, Povey, S, Fisher, R A, Pickthall, V J

    Published in Annals of human genetics (01-07-1982)
    “…An investigation of 50 histologically complete hydatidiform moles was made by examining the molar tissue after termination of pregnancy. Attempts were made to…”
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    Simultaneous application of immunolabelling and in situ hybridization to detect the origin of B and T lymphocytes in a case of acute lymphocytic leukaemia after bone marrow transplantation by Khokhar, M T, Lawler, S D, Reeves, B R, Powles, R

    Published in Bone marrow transplantation (Basingstoke) (01-07-1989)
    “…Previous cytogenetic studies, using selective mitogens, on a patient with B cell acute lymphocytic leukaemia during the 6 years of remission after bone marrow…”
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    Monosomy 7 in childhood: a myeloproliferative disorder by Sieff, C A, Chessells, J M, Harvey, B A, Pickthall, V J, Lawler, S D

    Published in British journal of haematology (01-10-1981)
    “…Between 1976 and 1979 a myeloproliferative disease associated with cells monosomic for chromosome number 7 in the bone marrow was seen in six boys aged 5 1/2…”
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    Long-term effects of chemotherapy on lymphocyte chromosomes from patients treated for gestational trophoblastic tumours by REEVES, B. R, LAWLER, S. D, CASEY, G, HARRIS, H

    Published in British journal of cancer (01-11-1985)
    “…A cytogenetic follow-up study of patients treated with chemotherapy for gestational trophoblastic tumours was undertaken. In some cases, high levels of…”
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    One haplotype matched bone marrow grafts: an investigation using the HLA system as a marker of cellular origin by Jones, E H, Lawler, S D, Powles, R L

    Published in Disease markers (01-03-1988)
    “…HLA antigens were used as markers to study the lymphocyte population in 31 patients with leukaemia, treated with a one-haplotype matched bone marrow transplant…”
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    Genetic studies on hydatidiform moles by Lawler, S D

    “…Using an historical approach, this article describes how genetic studies have elucidated the two entities into which the syndrome of hydatidiform mole can now…”
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