Preimplantation genetic diagnosis for hemophilia A using indirect linkage analysis and direct genotyping approaches von LAURIE, A. D., HILL, A. M., HARRAWAY, J. R., FELLOWES, A. P., PHILLIPSON, G. T., BENNY, P. S., SMITH, M. P., GEORGE, P. M.

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Homozygous truncation of the fibrinogen Aα chain within the coiled coil causes congenital afibrinogenemia von FELLOWES, A. P, BRENNAN, S. O, HOLME, R, STORMORKEN, H, BROSSTAD, F. R, GEORGE, P. M

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Identification and Characterization of Five New Fibrinogen Gene Polymorphisms von FELLOWES, ANDREW P., BRENNAN, STEPHEN O., GEORGE, PETER M.

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Simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations von STOTT, M. K, FELLOWES, A. P, UPTON, J. D, BURT, M. J, GEORGE, P. M

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Electrospray ionization mass spectrometry identification of fibrinogen Banks Peninsula (γ280Tyr→Cys): a new variant with defective polymerization von Fellowes, Andrew P., Brennan, Stephen O., Ridgway, Hayley J., Heaton, David C., George, Peter M.

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Hypofibrinogenemia in an individual with 2 coding (γ82 A→G and Bβ235 P→L) and 2 noncoding mutations von Brennan, Stephen O., Fellowes, Andrew P., Faed, James M., George, Peter M.

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Molecular Mechanisms of Hypo- and Afibrinogenemia von BRENNAN, STEPHEN O., FELLOWES, ANDREW P., GEORGE, PETER M.

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Nucleotide sequence of the coat protein gene of a necrotic strain of potato virus Y from New Zealand von Hay, J.M, Fellowes, A.P, Timmerman, G.M

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Correction for Stott et al.: simple multiplex PCR for the simultaneous detection of the C282Y and H63D hemochromatosis (HFE) gene mutations von Stott, M K, Fellowes, A P, Upton, J D, Burt, M J, George, P M

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Rapid detection of the fibrinogen A alpha 16Arg --> His mutation von Ridgway, H J, Brennan, S O, Fellowes, A P, George, P M

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Apolipoprotein B-32: a new truncated mutant of human apolipoprotein B capable of forming particles in the low density lipoprotein range von McCormick, Sally P.A., Fellowes, Andrew P., Walmsley, Trever A., George, Peter M.

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A Novel Variant of Transthyretin (Prealbumin), Thr119 to Met, Associated with Increased Thyroxine Binding von Scrimshaw, B J, Fellowes, A P, Palmer, B N, Croxson, M S, Stockigt, J R, George, P M

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Rapid detection of the fibrinogen Aα16Arg→His mutation von RIDGWAY, H. J, BRENNAN, S. O, FELLOWES, A. P, GEORGE, P. M

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Albumin Hawkes Bay; a low level variant caused by loss of a sulphydryl group at position 177 von Brennan, Stephen O., Fellowes, Andrew P.

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Albumin Rugby Park: a truncated albumin variant caused by a G → C splice-site mutation in nitro 13 von Peach, R.J., Fellowes, A.P., Brennan, S.O., George, P.M.

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Albumin Rugby Park : a truncated albumin variant caused by a G → C splice-site mutation in intron 13 von PEACH, R. J, FELLOWES, A. P, BRENNAN, S. O, GEORGE, P. M

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Nucleotide sequences of the coat protein gene of a necrotic strain of potato virus Y from New Zealand von Hay, J M, Fellowes, A P, Timmerman, G M

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Towards V-based high-entropy alloys for nuclear fusion applications von Barron, P.J., Carruthers, A.W., Fellowes, J.W., Jones, N.G., Dawson, H., Pickering, E.J.

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Homologous Recombination Repair Deficiency: An Overview for Pathologists von Doig, Kenneth D., Fellowes, Andrew P., Fox, Stephen B.

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Profound MEK inhibitor response in a cutaneous melanoma harboring a GOLGA4-RAF1 fusion von McEvoy, Christopher R, Xu, Huiling, Smith, Kortnye, Etemadmoghadam, Dariush, San Leong, Huei, Choong, David Y, Byrne, David J, Iravani, Amir, Beck, Sophie, Mileshkin, Linda, Tothill, Richard W, Bowtell, David D, Bates, Bindi M, Nastevski, Violeta, Browning, Judy, Bell, Anthony H, Khoo, Chloe, Desai, Jayesh, Fellowes, Andrew P, Fox, Stephen B, Prall, Owen Wj

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