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	141.	Biochemical markers of trisomy 21 and the pathophysiology of Down's syndrome pregnancies. [electronic resource] by Newby, D Aitken, D A Crossley, J A Howatson, A G Macri, J N Connor, J M Producer: 19980210 In: Prenatal diagnosis vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	142.	Methylene tetrahydrofolate reductase (MTHFR) and nitric oxide synthase (ecNOS) genes and risks of peripheral arterial disease and coronary heart disease: Edinburgh Artery Study. [electronic resource] by Fowkes, F G Lee, A J Hau, C M Cooke, A Connor, J M Lowe, G D Producer: 20000531 In: Atherosclerosis vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	143.	Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions. [electronic resource] by Connor, J M Pirrit, L A Yates, J R Crossley, J A Imrie, S J Colgan, J M Producer: 19870320 In: Journal of medical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	144.	Application of an intragenic genomic probe to genetic counselling for haemophilia B in the west of Scotland. [electronic resource] by Connor, J M Pettigrew, A F Hann, I M Forbes, C D Lowe, G D Affara, N A Producer: 19860128 In: Journal of medical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	145.	First-trimester biochemical screening for fetal chromosome abnormalities and neural tube defects. [electronic resource] by Aitken, D A McCaw, G Crossley, J A Berry, E Connor, J M Spencer, K Macri, J N Producer: 19940217 In: Prenatal diagnosis vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	146.	Detection of Y mosaicism in patients with Turner's syndrome. [electronic resource] by Chu, C E Connor, J M Donaldson, M D Kelnar, C J Smail, P J Greene, S A 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)
	147.	Second-trimester pregnancy associated plasma protein-A levels are reduced in Cornelia de Lange syndrome pregnancies. [electronic resource] by Aitken, D A Ireland, M Berry, E Crossley, J A Macri, J N Burn, J Connor, J M Producer: 19991109 In: Prenatal diagnosis vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	148.	Evidence for genetic heterogeneity in tuberous sclerosis. [electronic resource] by Sampson, J R Yates, J R Pirrit, L A Fleury, P Winship, I Beighton, P Connor, J M Producer: 19891003 In: Journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	149.	Expression and loss of heterozygosity of c-met proto-oncogene in primary breast cancer. [electronic resource] by Nagy, J Clark, J S Cooke, A Campbell, A M Connor, J M Purushotham, A D George, W D Producer: 19951107 In: Journal of surgical oncology vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	150.	Acute intermittent porphyria: the in vitro expression of mutant hydroxymethylbilane synthase. [electronic resource] by Ong, P M Lanyon, W G Graham, G Hift, R J Halkett, J Moore, M R Connor, J M Producer: 19971029 In: Molecular and cellular probes vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	151.	Demystification of Chester porphyria: a nonsense mutation in the Porphobilinogen Deaminase gene. [electronic resource] by Poblete-Gutiérrez, P Wiederholt, T Martinez-Mir, A Merk, H F Connor, J M Christiano, A M Frank, J Producer: 20070529 In: Physiological research vol. 55 Suppl 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	152.	Detection of four mutations in six unrelated South African patients with acute intermittent porphyria. [electronic resource] by Ong, P M Lanyon, W G Hift, R J Halkett, J Moore, M R Mgone, C S Connor, J M Producer: 19960819 In: Molecular and cellular probes vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	153.	Identification of two novel mutations in the hydroxymethylbilane synthase gene in three patients from two unrelated families with acute intermittent porphyria. [electronic resource] by Ong, P M Lanyon, W G Hift, R J Halkett, J Cramp, C E Moore, M R Connor, J M Producer: 19980226 In: Human heredity vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	154.	Linkage analysis in the fragile X syndrome using multiple distal Xq polymorphic DNA markers. [electronic resource] by Glass, I A Pirrit, L A White, E M Bell, M V Davies, K E Cockburn, F Connor, J M Producer: 19910521 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)
	155.	First trimester biochemical screening for trisomy 21: the role of free beta hCG, alpha fetoprotein and pregnancy associated plasma protein A. [electronic resource] by Spencer, K Aitken, D A Crossley, J A McCaw, G Berry, E Anderson, R Connor, J M Macri, J N Producer: 19950221 In: Annals of clinical biochemistry vol. 31 ( Pt 5) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	156.	The angiotensin I converting enzyme gene and predisposition to high blood pressure. [electronic resource] by Harrap, S B Davidson, H R Connor, J M Soubrier, F Corvol, P Fraser, R Foy, C J Watt, G C Producer: 19930429 In: Hypertension (Dallas, Tex. : 1979) vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	157.	Possible role of imprinting in the Turner phenotype. [electronic resource] by Chu, C E Donaldson, M D Kelnar, C J Smail, P J Greene, S A Paterson, W F Connor, J M Producer: 19950316 In: Journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	158.	Lethal neonatal chondrodysplasias in the West of Scotland 1970-1983 with a description of a thanatophoric, dysplasialike, autosomal recessive disorder, Glasgow variant. [electronic resource] by Connor, J M Connor, R A Sweet, E M Gibson, A A Patrick, W J McNay, M B Redford, D H Producer: 19851118 In: American journal of medical genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	159.	Evidence that the gene for tuberous sclerosis is on chromosome 9. [electronic resource] by Fryer, A E Chalmers, A Connor, J M Fraser, I Povey, S Yates, A D Yates, J R Osborne, J P Producer: 19870427 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	160.	Detection of a 15q deletion in a child with Angelman syndrome by cytogenetic analysis and flow cytometry. [electronic resource] by Cooke, A Tolmie, J L Glencross, F J Boyd, E Clarke, M M Day, R Stephenson, J B Connor, J M Producer: 19890927 In: American journal of medical genetics vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 183 results.