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	35761.	Polymorphic variability in the exon 19 of the RB1 gene and its flanking intronic sequences in HPV16-associated precancerous lesions in the Greek population. [electronic resource] by Tsakogiannis, D Moschonas, G D Daskou, M Stylianidou, Z Kyriakopoulou, Z Kottaridi, C Dimitriou, T G Gartzonika, C Markoulatos, P Producer: 20181107 In: Journal of medical microbiology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35762.	The UCP2-866G/A Polymorphism Could be Considered as a Genetic Marker of Different Functional Prognosis in Ischemic Stroke After Recanalization. [electronic resource] by Díaz-Maroto Cicuéndez, I Fernández-Díaz, E García-García, J Jordán, J Fernández-Cadenas, I Montaner, J Serrano-Heras, G Segura, T Producer: 20180718 In: Neuromolecular medicine vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35763.	Association of OX40 gene polymorphisms (rs17568G/A and rs229811A/C) with head and neck squamous cell carcinoma. [electronic resource] by Faghih, Zahra Abtahi, Shabnam Khademi, Bijan Nikfarjam, Farzaneh Erfani, Nasrollah Producer: 20200106 In: Molecular biology reports vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35764.	The Relationship Between eNOS Polymorphisms With Age, Smoking, Body Mass Index, and Clinicopathologic Parameters in Patients With Breast Cancer in Comparison With a Control Group. [electronic resource] by Fard, Zahra Tahmasebi Producer: 20210621 In: Clinical breast cancer vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35765.	Pelizaeus-Merzbacher disease: detection of mutations Thr181----Pro and Leu223----Pro in the proteolipid protein gene, and prenatal diagnosis. [electronic resource] by Strautnieks, S Rutland, P Winter, R M Baraitser, M Malcolm, S Producer: 19921028 In: American journal of human genetics vol. 51 Availability: No items available. Save to lists Add to cart (remove)
	35766.	cDNA cloning of mouse NKR-P1 and genetic linkage with LY-49. Identification of a natural killer cell gene complex on mouse chromosome 6. [electronic resource] by Yokoyama, W M Ryan, J C Hunter, J J Smith, H R Stark, M Seaman, W E Producer: 19911119 In: Journal of immunology (Baltimore, Md. : 1950) vol. 147 Availability: No items available. Save to lists Add to cart (remove)
	35767.	Gene therapy for X-linked immunodeficiencies. [electronic resource] by Kinnon, C O'Reilly, M A Pelham, A Malcolm, S Porter, C D Parkar, M H Collins, M K Leveinsky, R J Producer: 19911203 In: Allergologia et immunopathologia vol. 19 Availability: No items available. Save to lists Add to cart (remove)
	35768.	Oncogenes of stomach cancers. [electronic resource] by Terada, M Hattori, Y Yoshida, T Sakamoto, H Katoh, O Wada, A Yokota, J Sugimura, T Producer: 19900524 In: Basic life sciences vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35769.	Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1. [electronic resource] by Li, S Crenshaw, E B Rawson, E J Simmons, D M Swanson, L W Rosenfeld, M G Producer: 19901121 In: Nature vol. 347 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35770.	Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms. [electronic resource] by Balsamo, A Revelli, A Borelli, I Amoroso, A Cenderelli, G De Sanso, G Mazzola, G Curtoni, E S Zoppetti, G Massobrio, M Producer: 19920911 In: Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35771.	A molecular analysis of the telomeric end of the major histocompatibility complex. DNA typing of HLA-A3 subtypes and -B7. [electronic resource] by Dorak, M T Wilson, D W Galbraith, I Henderson, N Burnett, A K Worwood, M Producer: 19950622 In: Human immunology vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35772.	Enhancer-trap targeting at the Broad-Complex locus of Drosophila melanogaster. [electronic resource] by Gonzy-Tréboul, G Lepesant, J A Deutsch, J Producer: 19950615 In: Genes & development vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35773.	Prenatal diagnosis in known fragile X carriers. [electronic resource] by Maddalena, A Hicks, B D Spence, W C Levinson, G Howard-Peebles, P N Producer: 19941116 In: American journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35774.	Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia. [electronic resource] by Mannens, M Hoovers, J M Redeker, E Verjaal, M Feinberg, A P Little, P Boavida, M Coad, N Steenman, M Bliek, J Producer: 19940830 In: European journal of human genetics : EJHG vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35775.	Ceruloplasmin gene defect associated with epilepsy in EL mice. [electronic resource] by Garey, C E Schwarzman, A L Rise, M L Seyfried, T N Producer: 19940912 In: Nature genetics vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35776.	Structure of the promoter and genomic organization of the human beta'-adaptin gene (BAM22) from chromosome 22q12. [electronic resource] by Peyrard, M Pan, H Q Kedra, D Fransson, I Swahn, S Hartman, K Clifton, S W Roe, B A Dumanski, J P Producer: 19970212 In: Genomics vol. 36 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35777.	Mutations in the XPD gene leading to xeroderma pigmentosum symptoms. [electronic resource] by Kobayashi, T Kuraoka, I Saijo, M Nakatsu, Y Tanaka, A Someda, Y Fukuro, S Tanaka, K Producer: 19970626 In: Human mutation vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35778.	CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus. [electronic resource] by Donner, H Rau, H Walfish, P G Braun, J Siegmund, T Finke, R Herwig, J Usadel, K H Badenhoop, K Producer: 19970130 In: The Journal of clinical endocrinology and metabolism vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35779.	HLA-DQ beta 1 typing and non-Asp57 alleles in the aborigine population of Senegal. [electronic resource] by Chauffert, M Cisse, A Chevenne, D Parfait, B Michel, S Trivin, F Producer: 19960325 In: Diabetes care vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35780.	Thiopurine S-methyltransferase deficiency: two nucleotide transitions define the most prevalent mutant allele associated with loss of catalytic activity in Caucasians. [electronic resource] by Tai, H L Krynetski, E Y Yates, C R Loennechen, T Fessing, M Y Krynetskaia, N F Evans, W E Producer: 19960718 In: American journal of human genetics vol. 58 Availability: No items available. Save to lists Add to cart (remove)

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