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Journal of Medical Genetics|September 18, 2007
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisationK Osoegawa, G M Vessere, K H Utami, et al.Nature Nanotechnology|May 22, 2023
Scalable CMOS back-end-of-line-compatible AlScN/two-dimensional channel ferroelectric field-effect transistorsKwan-Ho Kim, Seyong Oh, Merrilyn Mercy Adzo Fiagbenu, et al.Journal of Medical Genetics|July 11, 2006
Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignanciesS-M Karppinen, R B Barkardottir, K Backenhorn, et al.Journal of Medical Genetics|February 4, 2005
Classification of BRCA1 missense variants of unknown clinical significanceC M Phelan, V Dapic, B Tice, et al.European Journal of Human Genetics : EJHG|October 20, 2000
Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in FinlandL Sarantaus, P Huusko, H Eerola, et al.Ecological Applications : a Publication of the Ecological Society of America|May 5, 2010
Marine reserves: fish life history and ecological traits matterJ Claudet, C W Osenberg, P Domenici, et al.Cell Metabolism|January 4, 2011
A common variant in TFB1M is associated with reduced insulin secretion and increased future risk of type 2 diabetesThomas Koeck, Anders H Olsson, Marloes Dekker Nitert, et al.Human Molecular Genetics|December 26, 2001
DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesisM Esteller, M F Fraga, M Guo, et al.Archives of Disease in Childhood|January 21, 2026
UK consensus guidelines for multidisciplinary care of children and young people with achondroplasia: a modified Delphi processToby P Candler, Kate Ali, Emma Bewick, et al.Cancer Research|March 21, 1998
Consortium study on 1280 breast carcinomas: allelic loss on chromosome 17 targets subregions associated with family history and clinical parametersC M Phelan, A Borg, M Cuny, et al.Pageof 71