Publications Archives Toutes les publications 2024 2023 2022 2021 2020 2019 2018 2017 2016 2015 2014 2013 2012 2011 2010 2009 2008 2007 2006 2005 2004 2003 2002 2001 2000 1999 1998 1997 1996 1995 1994 1993 1992 1991 1990 Evidence of founder chromosomes in fragile X syndrome. Richards RI, Holman K, Friend K, Kremer E, Hillen D, Staples A, Brown WT, Goonewardena P, Tarleton J, Schwartz C. Nature genetics. 1 1992 Fragile-X syndrome: unique genetics of the heritable unstable element Yu S, Mulley J, Loesch D, Turner G, Donnelly A, Gedeon A, Hillen D, Kremer E, Lynch M, Pritchard M. American journal of human genetics. 1992 The gene for the human IgA Fc receptor maps to 19q13.4. Kremer EJ, Kalatzis V, Baker E, Callen DF, Sutherland GR, Maliszewski CR. Human genetics. 1992 Analysis of the promoter for the gene encoding the testis-specific histone H1t in a somatic cell line: evidence for cell-cycle regulation and modulation by distant upstream sequences. Kremer EJ, Kistler WS. Gene. 1992 Prenatal diagnosis of fragile X syndrome by direct detection of the unstable DNA sequence. Sutherland GR, Gedeon A, Kornman L, Donnelly A, Byard RW, Mulley JC, Kremer E, Lynch M, Pritchard M, Yu S. The New England journal of medicine. 1991 Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site. Richards RI, Holman K, Kozman H, Kremer E, Lynch M, Pritchard M, Yu S, Mulley J, Sutherland GR. Journal of medical genetics. 1991 Localization of mRNA for testis-specific histone H1t by in situ hybridization. Kremer EJ, Kistler WS. Experimental cell research. 1991 Isolation of a human DNA sequence which spans the fragile X. Kremer EJ, Yu S, Pritchard M, Nagaraja R, Heitz D, Lynch M, Baker E, Hyland VJ, Little RD, Wada M. American journal of human genetics. 1991 Hereditary unstable DNA: a new explanation for some old genetic questions? Sutherland GR, Haan EA, Kremer E, Lynch M, Pritchard M, Yu S, Richards RI. Lancet (London, England). 1991 Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n Kremer EJ, Pritchard M, Lynch M, Yu S, Holman K, Baker E, Warren ST, Schlessinger D, Sutherland GR, Richards RI. Science (New York, N.Y.). 1991 Fragile X genotype characterized by an unstable region of DNA Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D. Science (New York, N.Y.). 1991 Isolation of a genomic clone encoding the rat histone variant, H1d. Cole KD, Kandala JC, Kremer E, Kistler WS. Gene. 1990 Précédent 1 2 … 39 40 41 42