Your search returned 42 results.

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	1.	Molecular diagnosis of the fragile X [Fra (X)] syndrome: calculation of risks based on flanking DNA markers in small phase-unknown families. [electronic resource] by Bridge, P J Lillicrap, D P Producer: 19890814 In: American journal of medical genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Prolonged thrombocytopenia in post-transfusion purpura (PTP) associated with changes in the crossed immunoelectrophoretic pattern of von Willebrand factor (vWF), circulating immune complexes and endothelial cell cytotoxicity. [electronic resource] by Lillicrap, D P Ford, P M Giles, A R Producer: 19860307 In: British journal of haematology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Somatic mosaicism and female-to-female transmission in a kindred with hemophilia B (factor IX deficiency). [electronic resource] by Taylor, S A Deugau, K V Lillicrap, D P Producer: 19910214 In: Proceedings of the National Academy of Sciences of the United States of America vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Relapse of acute myelogenous leukemia presenting with extrahepatic obstruction of the biliary tract. [electronic resource] by Lillicrap, D P Ginsburg, A D Corbett, W E Producer: 19830127 In: Canadian Medical Association journal vol. 127 Availability: No items available. Save to lists Add to cart (remove)
	5.	Multicentric warfarin-induced skin necrosis complicating heparin-induced thrombocytopenia. [electronic resource] by Warkentin, T E Sikov, W M Lillicrap, D P Producer: 19990930 In: American journal of hematology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A BstXI polymorphism detected by the factor VIII genomic probe p.482.6 (F8C). [electronic resource] by Taylor, S A Bridge, P J Lillicrap, D P Producer: 19890929 In: Nucleic acids research vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Carrier detection and prenatal diagnosis of Pelizaeus-Merzbacher disease using a combination of anonymous DNA polymorphisms and the proteolipid protein (PLP) gene cDNA. [electronic resource] by Bridge, P J MacLeod, P M Lillicrap, D P Producer: 19910807 In: American journal of medical genetics vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	An association between the common hereditary hemochromatosis mutation and the factor V Leiden allele in a population with thrombosis. [electronic resource] by Xie, Y G Lillicrap, D P Taylor, S A Producer: 19980910 In: Blood vol. 92 Availability: No items available. Save to lists Add to cart (remove)
	9.	Association of lupus anticoagulant with severe valvular heart disease in systemic lupus erythematosus. [electronic resource] by Ford, P M Ford, S E Lillicrap, D P Producer: 19880907 In: The Journal of rheumatology vol. 15 Availability: No items available. Save to lists Add to cart (remove)
	10.	Organization of a hemophilia genetic screening program. Ontario Hemophilia Study Group. [electronic resource] by Lillicrap, D P Bridge, P J Giles, A R Producer: 19900409 In: Progress in clinical and biological research vol. 324 Availability: No items available. Save to lists Add to cart (remove)
	11.	Synergy between transcription factors DBP and C/EBP compensates for a haemophilia B Leyden factor IX mutation. [electronic resource] by Picketts, D J Lillicrap, D P Mueller, C R Producer: 19930629 In: Nature genetics vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Inherited thrombocytopenia, elevated serum IgA and renal disease: identification as a variant of the Wiskott-Aldrich syndrome. [electronic resource] by Standen, G R Lillicrap, D P Matthews, N Bloom, A L Producer: 19860926 In: The Quarterly journal of medicine vol. 59 Availability: No items available. Save to lists Add to cart (remove)
	13.	Premature stroke in a family with lupus anticoagulant and antiphospholipid antibodies. [electronic resource] by Ford, P M Brunet, D Lillicrap, D P Ford, S E Producer: 19900305 In: Stroke vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Gonadal mosaicism in a family with adrenoleukodystrophy: molecular diagnosis of carrier status among daughters of a gonadal mosaic when direct detection of the mutation is not possible. [electronic resource] by Graham, G E MacLeod, P M Lillicrap, D P Bridge, P J Producer: 19920617 In: Journal of inherited metabolic disease vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Erythroblast multinuclearity in bone marrow and spleen. Congenital dyserythropoietic anemia-like abnormalities without functional evidence of dyserythropoiesis. [electronic resource] by Lillicrap, D P Corbett, W E Giles, A R Ginsburg, A D Producer: 19870618 In: Archives of pathology & laboratory medicine vol. 111 Availability: No items available. Save to lists Add to cart (remove)
	16.	Carrier detection in the hemophilias. [electronic resource] by Lillicrap, D P White, B N Holden, J J Giles, A R Producer: 19871209 In: American journal of hematology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Sensitivity of PCR in detecting monoclonal B cell proliferations. [electronic resource] by Ling, F C Clarke, C E Corbett, W E Lillicrap, D P Producer: 19940516 In: Journal of clinical pathology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Heterogeneity of laboratory test results for antiphospholipid antibodies in patients treated with chlorpromazine and other phenothiazines. [electronic resource] by Lillicrap, D P Pinto, M Benford, K Ford, P M Ford, S Producer: 19900703 In: American journal of clinical pathology vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Defective propeptide processing and abnormal activation underlie the molecular pathology of factor IX Troed-y-Rhiw. [electronic resource] by Liddell, M B Lillicrap, D P Peake, I R Bloom, A L Producer: 19890918 In: British journal of haematology vol. 72 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation. [electronic resource] by Brown, K Luddington, R Taylor, S A Lillicrap, D P Baglin, T P Producer: 19990610 In: British journal of haematology vol. 105 Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 42 results.