Search Results - "Davison, E V"

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  1. 1

    Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta‐analysis by Hillman, S. C., Pretlove, S., Coomarasamy, A., Mcmullan, D. J., Davison, E. V., Maher, E. R., Kilby, M. D.

    Published in Ultrasound in obstetrics & gynecology (01-01-2011)
    “…Objective Array comparative genomic hybridization (CGH) is transforming clinical cytogenetics with its ability to interrogate the human genome at increasingly…”
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  2. 2

    Rapid prenatal diagnosis of common trisomies: discordant results between QF-PCR analysis and karyotype analysis on long-term culture for a case of trisomy 18 detected in CVS by Allen, S. K., Luharia, A., Gould, C. P., MacDonald, F., Larkins, S., Davison, E. V.

    Published in Prenatal diagnosis (01-12-2006)
    “…Objectives QF‐PCR analysis can be used as a rapid test to diagnose primary trisomy in prenatal samples. Mosaicism in CVS detected by QF‐PCR has previously been…”
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  3. 3

    Confined placental mosaicism, IUGR, and adverse pregnancy outcome: a controlled retrospective U.K. collaborative survey by Wolstenholme, J, Rooney, D E, Davison, E V

    Published in Prenatal diagnosis (01-05-1994)
    “…In a retrospective collaborative study involving 21 U.K. laboratories and 11,775 CVS prenatal diagnostic procedures, a total of 73 cases of confined placental…”
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  4. 4

    A further case of confined placental mosaicism for trisomy 2 associated with adverse pregnancy outcome by Roberts, Eileen, Dunlop, J., Davis, G. S., Churchill, D., Davison, E. V.

    Published in Prenatal diagnosis (01-07-2003)
    “…Objectives To add to the knowledge base concerning confined placental mosaicism for trisomy 2. Methods Cytogenetic study of a late CVS referred for…”
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  5. 5

    Epidermal mosaicism and Blaschko's lines by Moss, C, Larkins, S, Stacey, M, Blight, A, Farndon, P A, Davison, E V

    Published in Journal of medical genetics (01-09-1993)
    “…To test the hypothesis that epidermal rather than dermal mosaicism determines Blaschko's lines in hypomelanosis of Ito (HI), we studied the distribution of…”
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  6. 6

    First‐trimester prenatal diagnosis of a familial subtelomeric translocation by Kilby, M. D., Brackley, K. J., Walters, J. J., Morton, J., Roberts, E., Davison, E. V.

    Published in Ultrasound in obstetrics & gynecology (01-06-2001)
    “…A new fluorescent in situ hybridization (FISH) technique utilizes a complete set of telomeric probes to screen for deletions or rearrangements within the…”
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  7. 7

    STRUCTURAL CHROMOSOME ANOMALIES IN CONGENITAL DIAPHRAGMATIC HERNIA by HOWE, DAVID T., KILBY, MARK D., SIRRY, HATEM, BARKER, GILLIAN M., ROBERTS, EILEEN, DAVISON, E. VALERIE, MCHUGO, JOSEPHINE, WHITTLE, MARTIN J.

    Published in Prenatal diagnosis (01-11-1996)
    “…In order to determine the outcome and associated chromosomal and structural anomalies in fetuses diagnosed in utero as having a congenital diaphragmatic…”
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  8. 8

    Prenatal diagnosis of mosaicism for partial trisomy 8: a case report including fetal pathology by Jay, A., Kilby, M. D., Roberts, E., Brackley, K., Platt, C., McHugo, J., Davison, E. V.

    Published in Prenatal diagnosis (01-10-1999)
    “…A case of prenatally diagnosed partial trisomy 8 is described. The ‘syndrome’ is associated with skeletal and cardiac anomalies, as well as hepatic…”
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  9. 9

    Prospective Prenatal Diagnosis of Prader-Willi Syndrome due to Maternal Disomy for Chromosome 15 following Trisomic Zygote Rescue by Roberts, Eileen, Stevenson, K., Cole, T., Redford, D. H. A., Davison, E. V.

    Published in Prenatal diagnosis (01-08-1997)
    “…We present a prenatal predictive diagnosis of Prader–Willi syndrome arising as a result of maternal heterodisomy for chromosome 15. The diagnosis arose…”
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  10. 10
  11. 11

    Cytogenetic analysis of a granulocytic sarcoma in a patient without systemic leukaemia by Adam, L R, Angus, B, Carey, P, Davison, E V

    Published in Journal of clinical pathology (01-01-1991)
    “…Granulocytic sarcoma is a rare complication of leukaemia. Occasionally it presents before the development of systemic leukaemia when diagnosis may be…”
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  12. 12

    Adherence of staphylococcus aureus to influenza A virus-infected Madin-Darby canine kidney cell cultures by Davison, V E, Sanford, B A

    Published in Infection and Immunity (01-04-1981)
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  13. 13

    Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13) by GOLDMAN, A. S. H, MARTIN, R. H, JOHANNISSON, R, GOULD, C. P, DAVISON, E. V, EMSLIE, J. E, BURN, J, HULTEN, M. A

    Published in Journal of medical genetics (01-07-1992)
    “…A phenotypically normal male who fathered a son with the karyotype 46,XY,del(10)(p13) was found to be a balanced carrier of an inverted insertion (3;10)…”
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  14. 14

    A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome by Jefferson, R D, Burn, J, Gaunt, K L, Hunter, S, Davison, E V

    Published in Journal of medical genetics (01-10-1986)
    “…A female infant with peripheral pulmonary artery stenosis, growth retardation, and developmental delay was noticed to have facial features consistent with a…”
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  15. 15

    Partial trisomy 20p resulting from a recombination of a familial pericentric inversion by BOWN, N, CROSS, I, DAVISON, E. V, BURN, J

    Published in Human genetics (01-12-1986)
    “…Recombination of an inherited pericentric inversion of chromosome 20 has given rise to a child with partial trisomy 20p. To our knowledge no previous familial…”
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  16. 16

    Chromosome studies of males in an institution for the mentally handicapped by English, C J, Davison, E V, Bhate, M S, Barrett, L

    Published in Journal of medical genetics (01-06-1989)
    “…Karyotypes were examined in 512 (91.9%) of 557 male patients in an institution for the mentally handicapped. A total of 110 (21.5%) had an abnormal karyotype:…”
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  17. 17

    Chromosome 22 abnormalities in Ewing's sarcoma by Davison, E V, Pearson, A D, Emslie, J, Reid, M M, Malcolm, A, Craft, A W

    Published in Journal of clinical pathology (01-08-1989)
    “…A child with disseminated Ewing's sarcoma underwent cytogenetic investigations which showed different structural rearrangements of chromosome 22 at diagnosis…”
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  18. 18

    Partial trisomy 16 as a result of familial 16;20 translocation by Davison, E V, Beesley, J R

    Published in Journal of medical genetics (01-10-1984)
    “…Although trisomy 16 is well recognised in spontaneous abortuses, it is infrequent in livebirths and there is little information about the clinical effects. We…”
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  19. 19

    Staphylococcus aureus adherence to influenza A virus-infected and control cell cultures: evidence for multiple adhesins by Sanford, B A, Davison, V E, Ramsay, M A

    “…During major epidemics with influenza, there is an increased number of pneumonias due to Staphylococcus aureus with a subsequent high mortality rate. We have…”
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  20. 20

    Fibrinogen-mediated adherence of group A Streptococcus to influenza A virus-infected cell cultures by Sanford, B A, Davison, V E, Ramsay, M A

    Published in Infection and Immunity (01-11-1982)
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