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	21.	Identification of a deletion in the low density lipoprotein (LDL) receptor gene in a patient with familial hypercholesterolaemia. [electronic resource] by Horsthemke, B Kessling, A M Seed, M Wynn, V Williamson, R Humphries, S E Producer: 19851017 In: Human genetics vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Maternal leptin receptor gene variant Gln223Arg is not associated with variation in birth weight or maternal body mass index in UK and South Asian populations. [electronic resource] by Rand, L Winchester, E C Millwood, I Y Penny, M A Kessling, A M Producer: 20011214 In: International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Molecular genetic evidence for a founder effect in familial hypercholesterolemia among French Canadians. [electronic resource] by Bétard, C Kessling, A M Roy, M Chamberland, A Lussier-Cacan, S Davignon, J 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)
	24.	A PvuII polymorphism in the 5' flanking region of the apolipoprotein AIV gene: its use to study genetic variation determining serum lipid and apolipoprotein concentration. [electronic resource] by Kessling, A M Taylor, R Temple, A Hutson, J Hidalgo, A Humphries, S E Producer: 19880418 In: Human genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	The expression of PAX5 in human transitional cell carcinoma of the bladder: relationship with de-differentiation. [electronic resource] by Adshead, J M Ogden, C W Penny, M A Stuart, E T Kessling, A M Producer: 19990802 In: BJU international vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Conserved gene sequences for species identification: PCR analysis of the 3' UTR of the SON gene distinguishes human and other mammalian DNAs. [electronic resource] by Soteriou, B Fisher, R A Khan, I M Kessling, A M Archard, L C Buluwela, L Producer: 19951002 In: Forensic science international vol. 73 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Expression of the developmental and oncogenic PAX2 gene in human prostate cancer. [electronic resource] by Khoubehi, B Kessling, A M Adshead, J M Smith, G L Smith, R D Ogden, C W Producer: 20010614 In: The Journal of urology vol. 165 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	DNA polymorphisms of the apolipoprotein AII and AI-CIII-AIV genes: a study in men selected for differences in high-density-lipoprotein cholesterol concentration. [electronic resource] by Kessling, A M Rajput-Wiliams, J Bainton, D Scott, J Miller, N E Baker, I Humphries, S E Producer: 19880413 In: American journal of human genetics vol. 42 Availability: No items available. Save to lists Add to cart (remove)
	29.	Allelic variability in D21S11, but not in APP or APOE, is associated with cognitive decline in Down syndrome. [electronic resource] by Farrer, M J Crayton, L Davies, G E Oliver, C Powell, J Holland, A J Kessling, A M Producer: 19970731 In: Neuroreport vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	A phenocopy of type III dysbetalipoproteinemia occurring in a candidate family for a putative apo E receptor defect. [electronic resource] by Davignon, J Dallongeville, J Roederer, G Roy, M Fruchart, J C Kessling, A M Bouthillier, D Lussier-Cacan, S Producer: 19910821 In: Annals of medicine vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Polymorphisms and linkage disequilibrium in the COL6A1 and COL6A2 gene cluster: novel DNA polymorphisms in the region of a candidate gene for congenital heart defects in Down's syndrome. [electronic resource] by Davies, G E Howard, C M Gorman, L M Farrer, M J Holland, A J Williamson, R Kessling, A M Producer: 19930305 In: Human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Molecular mapping of Alzheimer-type dementia in Down's syndrome. [electronic resource] by Prasher, V P Farrer, M J Kessling, A M Fisher, E M West, R J Barber, P C Butler, A C Producer: 19980410 In: Annals of neurology vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	Apolipoprotein B gene variants are involved in the determination of serum cholesterol levels: a study in normo- and hyperlipidaemic individuals. [electronic resource] by Talmud, P J Barni, N Kessling, A M Carlsson, P Darnfors, C Bjursell, G Galton, D Wynn, V Kirk, H Hayden, M R Producer: 19871214 In: Atherosclerosis vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Unusual genotypes in the COL6A1 gene in parents of children with trisomy 21 and major congenital heart defects. [electronic resource] by Davies, G E Howard, C M Farrer, M J Coleman, M M Cullen, L M Williamson, R Wyse, R K Kessling, A M Producer: 19940601 In: Human genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis. [electronic resource] by Humphries, S E Kessling, A M Horsthemke, B Donald, J A Seed, M Jowett, N Holm, M Galton, D J Wynn, V Williamson, R Producer: 19850606 In: Lancet (London, England) vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect. [electronic resource] by Howard, C M Davies, G E Farrer, M J Cullen, L M Coleman, M M Williamson, R Wyse, R K Palmer, R Kessling, A M Producer: 19930809 In: American journal of human genetics vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	37.	The SON gene encodes a conserved DNA binding protein mapping to human chromosome 21. [electronic resource] by Khan, I M Fisher, R A Johnson, K J Bailey, M E Siciliano, M J Kessling, A M Farrer, M Carritt, B Kamalati, T Buluwela, L Producer: 19940805 In: Annals of human genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome). [electronic resource] by Davies, G E Howard, C M Farrer, M J Coleman, M M Bennett, L B Cullen, L M Wyse, R K Burn, J Williamson, R Kessling, A M Producer: 19951215 In: Annals of human genetics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome? [electronic resource] by Baptista, M J Fairbrother, U L Howard, C M Farrer, M J Davies, G E Trikka, D Maratou, K Redington, A Greve, G Njølstad, P R Kessling, A M Producer: 20010118 In: Human genetics vol. 107 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)