Zobrazeno 1 - 10
of 31
pro vyhledávání: '"R. T. Howell"'
Autor:
A. T. Doherty, R. T. Howell, L. A. Ellis, I. Bisbinas, I. D. Learmonth, R. Newson, C. P. Case
Publikováno v:
The Journal of Bone and Joint Surgery. British volume. :1075-1081
The long-term biological effects of wear debris are unknown. We have investigated whether there is any evidence of cumulative mutagenic damage in peripheral blood lymphocytes of patients undergoing revision arthroplasty of predominantly metal-on-plas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb909e813e7cc813c359ee4516d5331b
https://doi.org/10.1302/0301-620x.83b7.0831075
https://doi.org/10.1302/0301-620x.83b7.0831075
Autor:
R. T. Howell, Keith W. Brown, Ruth Newbury-Ecob, P J Ancliff, K. L. Greenhalgh, Ellen G Vernon, C C Verschuuren-Bemelmans, H G Brunner, A. Bottani
Publikováno v:
Journal of Medical Genetics, 39, 876-81
Journal of Medical Genetics, 39, 12, pp. 876-81
JOURNAL OF MEDICAL GENETICS, 39(12), 876-881. BMJ PUBLISHING GROUP
Journal of Medical Genetics, 39, 12, pp. 876-81
JOURNAL OF MEDICAL GENETICS, 39(12), 876-881. BMJ PUBLISHING GROUP
Item does not contain fulltext The thrombocytopenia-absent radius (TAR) syndrome is a congenital malformation syndrome characterised by bilateral absence of the radii and a thrombocytopenia. The lower limbs, gastrointestinal, cardiovascular, and othe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ccdcfee9df51e726797f180082b0e63
http://hdl.handle.net/2066/185509
http://hdl.handle.net/2066/185509
Publikováno v:
The Journal of bone and joint surgery. British volume. 83(7)
The long-term biological effects of wear debris are unknown. We have investigated whether there is any evidence of cumulative mutagenic damage in peripheral blood lymphocytes of patients undergoing revision arthroplasty of predominantly metal-on-plas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1157984df503c4d1ffa4fd145bb5f97a
https://pubmed.ncbi.nlm.nih.gov/11603526
https://pubmed.ncbi.nlm.nih.gov/11603526
Publikováno v:
Clinical dysmorphology. 6(2)
We report a child in whom we observed markedly increased genome-wide spontaneous chromosomal breakage in both leucocytes and fibroblasts associated with severe growth retardation, radial aplasia, leucopenia, mild hydrocephalus and an unusual trichody
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c1f08ac0feefbfa51d18cb34d0362b69
https://pubmed.ncbi.nlm.nih.gov/9134289
https://pubmed.ncbi.nlm.nih.gov/9134289
Autor:
M G, Rainey, P, Harrison, J M, Hows, P J, Kingston, P A, Burton, B W, Codling, R T, Howell, R R, Slade
Publikováno v:
Bone marrow transplantation. 17(6)
Myeloablation followed by haemopoietic reconstitution using autologous peripheral blood progenitor cells (PBPC) is applicable to some patients with CML, particularly where there is no allogeneic stem cell donor available, and interferon alpha has fai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c8d2e4f36db3b57011461de34b9ebeb7
https://pubmed.ncbi.nlm.nih.gov/8807117
https://pubmed.ncbi.nlm.nih.gov/8807117
A 7 year old boy is described with moderate learning disability, facial dysmorphism, and a de novo duplication of chromosome 2 (q11.2-q21). There are few published reports of proximal 2q duplication, and none reporting direct de novo duplication for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f523e076409f0f79f69587f26bb74171
https://europepmc.org/articles/PMC1051712/
https://europepmc.org/articles/PMC1051712/
Autor:
R. T. Howell, Teresa Davies
Publikováno v:
Prenatal diagnosis. 14(11)
Cultures of a chorion biopsy taken from a pregnancy at risk of Bloom's syndrome revealed the high sister chromatid exchange frequency diagnostic of this rare disorder. To obtain the result, cultures were grown under standard conditions, with the addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59794ee8563aa9b3b84bc05816e70c31
https://pubmed.ncbi.nlm.nih.gov/7877955
https://pubmed.ncbi.nlm.nih.gov/7877955
Particular regions of the X and Y chromosomes share DNA sequence homology to the extent that cross hybridisation occurs. Thus, chromosome painting with a whole Y chromosome probe consistently results in fluorescence on specific regions of the X chrom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f0955693efecf2b8da42d80ff761679
https://europepmc.org/articles/PMC1049743/
https://europepmc.org/articles/PMC1049743/
Autor:
R T Howell
Evaluation of chromatid aberrations induced in culture by DNA cross linking agents provides the most reliable method currently available for the diagnosis and exclusion of Fanconi's anaemia. However, at appropriate concentrations of clastogenic agent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2e22fa1d342b67e46aa673272ad34b
https://europepmc.org/articles/PMC1016957/
https://europepmc.org/articles/PMC1016957/
Publikováno v:
Journal of medical genetics. 27(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b2f833dc86186835e8a3d7adbd27af1
https://pubmed.ncbi.nlm.nih.gov/2213847
https://pubmed.ncbi.nlm.nih.gov/2213847