Zobrazeno 1 - 8
of 8
pro vyhledávání: '"D J, McMullan"'
Autor:
Vaiyapuri Sumathi, Ann Williams, R. J. Grimer, J McClure, D J McMullan, D. C. Mangham, A. M. Davies
Publikováno v:
Histopathology. 48:363-376
Aims : (i) To report on the routine use of the reverse transcriptase-polymerase chain reaction (RT-PCR) technique on decalcified or non-decalcified, formalin-fixed, paraffin-embedded tissue (FFPET) for translocation detection, with particular emphasi
Autor:
G. Wilson, David W. Rowe, J. Bryon, Nick Bown, Simon Cotterill, Michael J. Griffiths, Ann E. Watmore, Elisabeth Vandenberghe, Fiona M. Ross, John T. Reilly, D. J. McMullan, S. J. Vickers, David J. Bunyan
Publikováno v:
British Journal of Haematology. 111:1051-1056
Autor:
D. J. McMullan, David J. Bunyan, Elisabeth Vandenberghe, G. Wilson, Fiona M. Ross, Michael J. Griffiths, S. J. Vickers, Simon Cotterill, John T. Reilly, Nick Bown, J. Bryon, Ann E. Watmore, David W. Rowe
Publikováno v:
British Journal of Haematology. 111:1051-1056
The rearrangements t(8;21)(q22;22) and inv(16)(p13q22) are two of the most frequently seen in acute myeloid leukaemia (AML), accounting for 8% and 4% of cases respectively. Detection of these abnormalities is important for disease management as both
Autor:
D. J. McMullan
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 45:373-374
Autor:
S C, Hillman, D J, McMullan, G, Hall, F S, Togneri, N, James, E J, Maher, C H, Meller, D, Williams, R J, Wapner, E R, Maher, M D, Kilby
Publikováno v:
Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 41(6)
Chromosomal microarray analysis (CMA) is utilized in prenatal diagnosis to detect chromosomal abnormalities not visible by conventional karyotyping. A prospective cohort of women undergoing fetal CMA and karyotyping following abnormal prenatal ultras
Publikováno v:
BJOG : an international journal of obstetrics and gynaecology. 119(10)
Publikováno v:
Journal of medical genetics. 32(4)
A case of a 27 year old male with a duplication of part of the long arm of chromosome 22 (22q11.2-q13.1) together with a pericentric inversion of the same chromosome is reported. Particular phenotypic features of note include absence of speech, persi
Autor:
Gulnaz Begum, Fiona Clark, D. J. McMullan, Richard Lovell, Michael J. Griffiths, Mark Cook, C. Craddock, P Mahendra, Donald Milligan, Sudhir Tauro
Publikováno v:
Blood. 106:1776-1776
Serial analysis of haemopoietic chimerism can be used to predict outcome after allogeneic SCT using a RIC regimen and guide post-transplant intervention. Although alemtuzumab is increasingly used as a component of RIC regimens, there have been few st