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Results 11-20 of 22 (Search time: 0.001 seconds).
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First PublishedTitleAuthor(s)Type
1995Genetic counselling on brittle grounds: Recurring osteogenesis imperfecta due to parental mosaicism for a dominant mutationRaghunath, M; Mackay, K; Dalgleish, R; Steinmann, BJournal Article
1994A Gly859Ser substitution in the triple helical domain of the alpha 2 chain of type I collagen resulting in osteogenesis imperfecta type III in two unrelated individuals.Rose, NJ; Mackay, K; Byers, PH; Dalgleish, RJournal Article
Mar-1996Substitution of glycine-661 by serine in the α1(I) and α2(I) chains of type I collagen results in different clinical and biochemical phenotypesNuytinck, L; Renard, J-P; De Paepe A; Dalgleish, R; Spotila, L; Van Regemorter NJournal Article
Apr-1988Discordant expression of the G syndrome in monozygotic twins.Young, ID; Dalgleish, R; MacKay, EH; MacFadyen, UMJournal Article
Sep-2011Clarity and claims in variation/mutation databasing.Dalgleish, R; Oetting, WS; Auerbach, AD; Beckmann, JS; Cambon-Thomsen, A; Devereau, A; Greenblatt, MS; Patrinos, GP; Taylor, GR; Vihinen, M; Brookes, AJJournal Article
Jul-2011WAVe: web analysis of the variome.Lopes, P; Dalgleish, R; Oliveira, JLJournal Article
1999Hypophosphatasia: Diagnostic application of linked DNA markers in the dominantly inherited adult formIqbal, SJ; Plaha, DS; Linforth, GH; Dalgleish, RJournal Article
Aug-2011Bilateral consecutive rupture of the quadriceps tendon in a man with BstUI polymorphism of the COL5A1 gene.Dalgleish, RJournal Article
1-Jan-1997Assignment of secreted phosphoprotein 24 (SPP2) to human chromosome band 2q37 -> qter by in situ hybridizationSwallow, JE; Merrison, WK; Gill, PK; Harris, S; Dalgleish, RJournal Article
Jan-1988BglII RFLPs in the COL1A2 gene in the Finnish population - A commentDalgleish, RJournal Article