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British Journal of Pharmacology|July 23, 2014
Therapeutic perspectives of epigenetically active nutrientsM Remely, L Lovrecic, A L de la Garza, et al.BMC Ophthalmology|June 30, 2017
Cataract and optic disk drusen in a patient with glycogenosis and di George syndrome: clinical and molecular reportD Allegrini, S Penco, A Pece, et al.The Journal of International Medical Research|February 12, 2011
A case of lichen ruber planus in a patient with familial multiple sclerosisJ Sepić, S Ristić, O Perković, et al.Human Molecular Genetics|February 1, 1994
The gene for the familial form of incontinentia pigmenti (IP2) maps to the distal part of Xq28A Smahi, C Hyden-Granskog, B Peterlin, et al.Balkan Journal of Medical Genetics : BJMG|March 14, 2024
Preimplantation Genetic Testing within the Public Healthcare System in SloveniaM Volk, K Writzl, A Veble, et al.Genes, Chromosomes & Cancer|March 1, 1997
Loss of heterozygosity at 7q31 in breast cancer: results from an International Collaborative Study Group. The Breast Cancer Somatic Genetics ConsortiumP Devilee, J Hermans, J Eyfjörd, et al.British Journal of Cancer|June 9, 1999
European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables. Breast Cancer Somatic Genetics ConsortiumV Launonen, K Laake, P Huusko, et al.Genes, Chromosomes & Cancer|June 24, 1999
Loss of heterozygosity at 11q23.1 and survival in breast cancer: results of a large European study. Breast Cancer Somatic Genetics ConsortiumK Laake, V Launonen, D Niederacher, et al.Journal of Dental Research|February 25, 2014
Strong association of variants around FOXE1 and orofacial cleftingK U Ludwig, A C Böhmer, M Rubini, et al.American Journal of Human Genetics|November 15, 2000
Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by languageZ H Rosser, T Zerjal, M E Hurles, et al.Pageof 9