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	1.	Athens Declaration for Healthy Cities. [electronic resource] by Avŕamopoulos, D Asvall, J E Producer: 19990419 In: Journal of public health medicine vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	DNA polymorphisms in the 3' untranslated region of genes on human chromosome 21. [electronic resource] by Avramopoulos, D Chakravarti, A Antonarakis, S E Producer: 19930316 In: Genomics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Central nervous system involvement in four patients with Charcot-Marie-Tooth disease with connexin 32 extracellular mutations. [electronic resource] by Panas, M Karadimas, C Avramopoulos, D Vassilopoulos, D Producer: 19990107 In: Journal of neurology, neurosurgery, and psychiatry vol. 65 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes. [electronic resource] by Chen, H Lowther, W Avramopoulos, D Antonarakis, S E Producer: 19950224 In: Human mutation vol. 4 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Alzheimer's risk variants in the clusterin gene are associated with alternative splicing. [electronic resource] by Szymanski, M Wang, R Bassett, S S Avramopoulos, D Producer: 20130211 In: Translational psychiatry vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Normal phenotype with paternal uniparental isodisomy for chromosome 21. [electronic resource] by Blouin, J L Avramopoulos, D Pangalos, C Antonarakis, S E Producer: 19931119 In: American journal of human genetics vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	7.	Three novel mutations in the gap junction beta 1 (GJB1) gene coding region identified in Charcot-Marie-Tooth patients of Greek origin: T55I, R164Q, V120E. Mutation in brief no 236. Online. [electronic resource] by Karadimas, C Panas, M Chronopoulou, P Avramopoulos, D Vassilopoulos, D Producer: 19990610 In: Human mutation vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Apolipoprotein E and presenilin-1 genotypes in Huntington's disease. [electronic resource] by Panas, M Avramopoulos, D Karadima, G Petersen, M B Vassilopoulos, D Producer: 19991026 In: Journal of neurology vol. 246 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Apolipoprotein E allele distribution in parents of Down's syndrome children. [electronic resource] by Avramopoulos, D Mikkelsen, M Vassilopoulos, D Grigoriadou, M Petersen, M B Producer: 19960618 In: Lancet (London, England) vol. 347 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Polymorphic dinucleotide repeats at the D3S1417, D3S1418 and D12S271 loci. [electronic resource] by Talbot, C C Warren, A C Avramopoulos, D Antonarakis, S E Producer: 19931105 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Linkage mapping of the AML1 gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region. [electronic resource] by Avramopoulos, D Cox, T Blaschak, J E Chakravarti, A Antonarakis, S E Producer: 19921201 In: Genomics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	A novel zinc finger cDNA with a polymorphic pentanucleotide repeat (ATTTT)n maps on human chromosome 19p. [electronic resource] by Chen, H Kalaitsidaki, M Warren, A C Avramopoulos, D Antonarakis, S E Producer: 19930511 In: Genomics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Linkage mapping of the carbonyl reductase (CBR) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region. [electronic resource] by Avramopoulos, D Cox, T Forrest, G L Chakravarti, A Antonarakis, S E Producer: 19920730 In: Genomics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Linkage mapping of the cystathionine beta-synthase (CBS) gene on human chromosome 21 using a DNA polymorphism in the 3' untranslated region. [electronic resource] by Avramopoulos, D Cox, T Kraus, J P Chakravarti, A Antonarakis, S E 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)
	15.	Genetic determinants of neuroglobin transcription. [electronic resource] by Wang, R Halper-Stromberg, E Szymanski-Pierce, M Bassett, S S Avramopoulos, D Producer: 20140908 In: Neurogenetics vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Shared variance of oculomotor phenotypes in a large sample of healthy young men. [electronic resource] by Valakos, D Karantinos, T Evdokimidis, I Stefanis, N C Avramopoulos, D Smyrnis, N Producer: 20190306 In: Experimental brain research vol. 236 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Association between presenilin-1 polymorphism and maternal meiosis II errors in Down syndrome. [electronic resource] by Petersen, M B Karadima, G Samaritaki, M Avramopoulos, D Vassilopoulos, D Mikkelsen, M Producer: 20001024 In: American journal of medical genetics vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Mirror-symmetric duplicated chromosome 21q with minor proximal deletion, and with neocentromere in a child without the classical Down syndrome phenotype. [electronic resource] by Barbi, G Kennerknecht, I Wöhr, G Avramopoulos, D Karadima, G Petersen, M B Producer: 20000421 In: American journal of medical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Higher scores of self reported schizotypy in healthy young males carrying the COMT high activity allele. [electronic resource] by Avramopoulos, D Stefanis, N C Hantoumi, I Smyrnis, N Evdokimidis, I Stefanis, C N Producer: 20030225 In: Molecular psychiatry vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Schizophrenia-related RGS4 gene variations specifically disrupt prefrontal control of saccadic eye movements. [electronic resource] by Kattoulas, E Stefanis, N C Avramopoulos, D Stefanis, C N Evdokimidis, I Smyrnis, N Producer: 20120907 In: Psychological medicine vol. 42 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 54 results.