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PreviewIssue DateTitleAuthor(s)
2018Deleterious variation shapes the genomic landscape of introgressionKim, B.Y.; Huber, C.D.; Lohmueller, K.E.
2003The clinical geneticist and the "new genetics"Haan, E.
2015HENMT1 and piRNA stability are required for adult male germ cell transposon repression and to define the spermatogenic program in the mouseLim, S.; Qu, Z.; Kortschak, R.; Lawrence, D.; Geoghegan, J.; Hempfling, A.; Bergmann, M.; Goodnow, C.; Ormandy, C.; Wong, L.; Mann, J.; Scott, H.; Jamsai, D.; Adelson, D.; O'Bryan, M.
2017Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesStessman, H.; Xiong, B.; Coe, B.; Wang, T.; Hoekzema, K.; Fenckova, M.; Kvarnung, M.; Gerdts, J.; Trinh, S.; Cosemans, N.; Vives, L.; Lin, J.; Turner, T.; Santen, G.; Ruivenkamp, C.; Kriek, M.; Van Haeringen, A.; Aten, E.; Friend, K.; Liebelt, J.; et al.
2017YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunctionGabriele, M.; Vulto-van Silfhout, A.; Germain, P.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.; Stromme, P.; Rosenfeld, J.; Shao, Y.; Craigen, W.; Schaaf, C.; Rodriguez-Buritica, D.; et al.
2017Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domainsGeisheker, M.; Heymann, G.; Wang, T.; Coe, B.; Turner, T.; Stessman, H.; Hoekzema, K.; Kvarnung, M.; Shaw, M.; Friend, K.; Liebelt, J.; Barnett, C.; Thompson, E.; Haan, E.; Guo, H.; Anderlid, B.; Nordgren, A.; Lindstrand, A.; Vandeweyer, G.; Alberti, A.; et al.
2017Soil DNA metabarcoding and high-throughput sequencing as a forensic tool: considerations, potential limitations and recommendationsYoung, J.; Austin, J.; Weyrich, L.
2014Whole exome sequencing of extreme morbid obesity patients: translational implications for obesity and related disordersPaz-Filho, G.; Boguszewski, M.; Mastronardi, C.; Patel, H.; Johar, A.; Chuah, A.; Huttley, G.; Boguszewski, C.; Wong, M.; Arcos-Burgos, M.; Licinio, J.
1997High resolution characterisation of an interstitial deletion of less than 1.9Mb at 4p16.3 associated with Wolf-Hirschhorn SyndromeFang, Y.; Bain, S.; Haan, E.; Eyre, H.; MacDonald, M.; Wright, T.; Altherr, M.; Riess, O.; Sutherland, G.; Callen, D.
2014Fitness valleys constrain HIV-1's adaptation to its secondary chemokine coreceptorDa Silva, J.; Wyatt, S.