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	1.	Fetal haemophilia and allied bleeding disorders. [electronic resource] by Mibashan, R S Millar, D S Producer: 19840127 In: British medical bulletin vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Variation of site-specific methylation patterns in the factor VIII (F8C) gene in human sperm DNA. [electronic resource] by Millar, D S Krawczak, M Cooper, D N Producer: 19981023 In: Human genetics vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Screening for inversions in the factor VIII (F8) gene causing severe haemophilia A. [electronic resource] by Millar, D S Kakkar, V V Cooper, D N Producer: 19940912 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A distinct sequence (ATAAA)n separates methylated and unmethylated domains at the 5'-end of the GSTP1 CpG island. [electronic resource] by Millar, D S Paul, C L Molloy, P L Clark, S J Producer: 20000914 In: The Journal of biological chemistry vol. 275 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Fetal haematology in rhesus isoimmunisation. [electronic resource] by Nicolaides, K H Rodeck, C H Millar, D S Mibashan, R S Producer: 19850415 In: British medical journal (Clinical research ed.) vol. 290 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesion. [electronic resource] by Schwartz, M Cooper, D N Millar, D S Kakkar, V V Scheibel, E Producer: 19930305 In: Prenatal diagnosis vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Inherited factor X deficiency: molecular genetics and pathophysiology. [electronic resource] by Cooper, D N Millar, D S Wacey, A Pemberton, S Tuddenham, E G Producer: 19970808 In: Thrombosis and haemostasis vol. 78 Availability: No items available. Save to lists Add to cart (remove)
	8.	The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqI. [electronic resource] by Millar, D S Zoll, B Martinowitz, U Kakkar, V V Cooper, D N Producer: 19911030 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Prenatal exclusion of severe factor VII deficiency by DNA sequencing. [electronic resource] by Millar, D S Cooper, D N Kakkar, V V Schwartz, M Scheibel, E Producer: 19920618 In: Lancet (London, England) vol. 339 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy. [electronic resource] by Millar, D S Allgrove, J Rodeck, C Kakkar, V V Cooper, D N Producer: 19950309 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	11.	A novel missense mutation in the antithrombin III gene (Ser349----Pro) causing recurrent venous thrombosis. [electronic resource] by Grundy, C B Holding, S Millar, D S Kakkar, V V Cooper, D N Producer: 19920427 In: Human genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Carrier detection in haemophilia A by direct analysis of factor VIII gene lesions. [electronic resource] by Millar, D S Green, P J Zoll, B Kakkar, V V Cooper, D N Producer: 19910702 In: Human genetics vol. 87 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Population differences in the frequency of the factor V Leiden variant among people with clinically symptomatic protein C deficiency. [electronic resource] by Hallam, P J Millar, D S Krawczak, M Kakkar, V V Cooper, D N Producer: 19951122 In: Journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Inherited factor VII deficiency: molecular genetics and pathophysiology. [electronic resource] by Cooper, D N Millar, D S Wacey, A Banner, D W Tuddenham, E G Producer: 19970808 In: Thrombosis and haemostasis vol. 78 Availability: No items available. Save to lists Add to cart (remove)
	15.	A novel point mutation (Val 297-->Met) in the serine proteinase domain of protein C in a patient with both venous and arterial thromboembolic disease. [electronic resource] by Millar, D S Wacey, A I Voke, J Kakkar, V V Cooper, D N Producer: 19931201 In: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Solid-phase hybridization capture of low-abundance target DNA sequences: application to the polymerase chain reaction detection of Mycobacterium paratuberculosis and Mycobacterium avium subsp. silvaticum. [electronic resource] by Millar, D S Withey, S J Tizard, M L Ford, J G Hermon-Taylor, J Producer: 19950727 In: Analytical biochemistry vol. 226 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Normal blood cell values in the early mid-trimester fetus. [electronic resource] by Millar, D S Davis, L R Rodeck, C H Nicolaides, K H Mibashan, R S Producer: 19860306 In: Prenatal diagnosis vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Prenatal diagnosis of hereditary protein C deficiency. [electronic resource] by Mibashan, R S Millar, D S Rodeck, C H Nicolaides, K H Berger, A Seligsohn, U Producer: 19860107 In: The New England journal of medicine vol. 313 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism. [electronic resource] by Wieland, K Millar, D S Grundy, C B Mibashan, R S Kakkar, V V Cooper, D N Producer: 19910402 In: Human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Prenatal diagnosis of Glanzmann's thrombasthenia. [electronic resource] by Seligsohn, U Mibashan, R S Rodeck, C H Nicolaides, K H Millar, D S Coller, B S Producer: 19860129 In: Lancet (London, England) vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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