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D M Layton

Showing results (41-50 of 51) with videos related to

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British Journal of Haematology|December 1, 1994
Haemophagocytic lymphohistiocytosis: experience at two U.K. centresW J Hirst, D M Layton, S Singh, et al.
Archives of Disease in Childhood|April 1, 1992
Fetal leucocyte count in rhesus diseaseN P Davies, A G Buggins, R J Snijders, et al.
Analytical Biochemistry|October 25, 2001
Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell diseaseS F Ofori-Acquah, B N Green, S C Davies, et al.
British Journal of Haematology|October 1, 1990
Clinicopathological features of acute undifferentiated leukaemia with a stem cell phenotypeF Brito-Babapulle, H Pullon, D M Layton, et al.
Blood Cells, Molecules & Diseases|August 3, 2001
Rapid identification of hemoglobin variants by electrospray ionization mass spectrometryB J Wild, B N Green, E K Cooper, et al.
Blood|November 11, 1999
Reversal of metabolic block in glycolysis by enzyme replacement in triosephosphate isomerase-deficient cellsA Ationu, A Humphries, M R Lalloz, et al.
Human Reproduction (Oxford, England)|October 1, 1992
Preimplantation diagnosis of a human beta-globin transgene in biopsied trophectoderm cells and blastomeres of the mouse embryoS A Sheardown, I Findlay, A Turner, et al.
American Journal of Human Genetics|January 23, 1999
Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mappingM Ohadi, M R Lalloz, P Sham, et al.
Journal of Hepatology|February 12, 1998
Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosisC Datz, M R Lalloz, W Vogel, et al.
Human Genetics|April 4, 2000
Molecular analysis of the genotype-phenotype relationship in factor X deficiencyD S Millar, L Elliston, P Deex, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
British Journal of Haematology|December 1, 1994
Haemophagocytic lymphohistiocytosis: experience at two U.K. centresW J Hirst, D M Layton, S Singh, et al.
Archives of Disease in Childhood|April 1, 1992
Fetal leucocyte count in rhesus diseaseN P Davies, A G Buggins, R J Snijders, et al.
Analytical Biochemistry|October 25, 2001
Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell diseaseS F Ofori-Acquah, B N Green, S C Davies, et al.
British Journal of Haematology|October 1, 1990
Clinicopathological features of acute undifferentiated leukaemia with a stem cell phenotypeF Brito-Babapulle, H Pullon, D M Layton, et al.
Blood Cells, Molecules & Diseases|August 3, 2001
Rapid identification of hemoglobin variants by electrospray ionization mass spectrometryB J Wild, B N Green, E K Cooper, et al.
Blood|November 11, 1999
Reversal of metabolic block in glycolysis by enzyme replacement in triosephosphate isomerase-deficient cellsA Ationu, A Humphries, M R Lalloz, et al.
Human Reproduction (Oxford, England)|October 1, 1992
Preimplantation diagnosis of a human beta-globin transgene in biopsied trophectoderm cells and blastomeres of the mouse embryoS A Sheardown, I Findlay, A Turner, et al.
American Journal of Human Genetics|January 23, 1999
Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mappingM Ohadi, M R Lalloz, P Sham, et al.
Journal of Hepatology|February 12, 1998
Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosisC Datz, M R Lalloz, W Vogel, et al.
Human Genetics|April 4, 2000
Molecular analysis of the genotype-phenotype relationship in factor X deficiencyD S Millar, L Elliston, P Deex, et al.
Pageof 6