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 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
