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Results 81-90 of 112 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
1999Genomic structure and expression analysis of the spastic paraplegia gene, SPG7Settasatian, C.; Whitmore, S.; Crawford, J.; Bilton, R.; Cleton-Jansen, A.M.; Sutherland, G.; Callen, D.
2016A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shapeRied, J.; Jeff, J.; Chu, A.; Bragg-Gresham, J.; Van Dongen, J.; Huffman, J.; Ahluwalia, T.; Cadby, G.; Eklund, N.; Eriksson, J.; Esko, T.; Feitosa, M.; Goel, A.; Gorski, M.; Hayward, C.; Heard-Costa, N.; Jackson, A.; Jokinen, E.; Kanoni, S.; Kristiansson, K.; et al.
2011Identification of SOX3 as an XX male sex reversal gene in mice and humansSutton, E.; Hughes, J.; White, S.; Sekido, R.; Tan, J.; Arboleda, V.; Rogers, N.; Knower, K.; Rowley, L.; Eyre, H.; Rizzoti, K.; McAninch, D.; Golcalves, J.; Slee, J.; Turbitt, E.; Bruno, D.; Bengtsson, H.; Harley, V.; Vilain, E.; Sinclair, A.; et al.
1995FRAXE and mental retardationMulley, J.; Yu, S.; Loesch, D.; Hay, D.; Donnelly, A.; Gedeon, A.; Carbonell, P.; Lopez, I.; Glover, G.; Garbarron, I.; Yu, P.; Baker, E.; Haan, E.; Hockey, A.; Knight, S.; Daview, K.; Richards, R.; Sutherland, G.
2014Mitochondrial genome sequencing in mesolithic North East Europe unearths a new sub-clade within the broadly distributed human haplogroup C1Der Sarkissian, C.; Brotherton, P.; Balanovsky, O.; Templeton, J.; Llamas, B.; Soubrier, J.; Moiseyev, V.; Khartanovich, V.; Cooper, A.; Haak, W.; Genographic Consortium,; Achilli, A.
2014AmericaPlex26: a SNaPshot multiplex system for genotyping the main human mitochondrial founder lineages of the AmericasCoutinho, A.; Valverde, G.; Fehren-Schmitz, L.; Cooper, A.; Barreto Romero, M.; Flores Espinoza, I.; Llamas, B.; Haak, W.; Achilli, A.
1997Assignment of the Human CC Chemokine Gene TARC (SCYA17) to chromosome 16q13Nomiyama, H.; Imai, T.; Kusuda, J.; Miura, R.; Callen, D.; Yoshie, O.
1998PAK3 mutation in nonsyndromic X-linked mental retardationAllen, K.; Gleeson, J.; Bagrodia, S.; Partington, M.; MacMillan, J.; Cerione, R.; Mulley, J.; Walsh, C.
1998The identification and localisation of a human gene with sequence similarity to Polycomblike of Drosophila melanogasterCoulson, M.; Robert, S.; Eyre, H.; Saint, R.
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.