Multiplex ligation-dependent probe amplification using a completely synthetic probe set
Stern, Rowena F, Roberts, Roland G, Mann, Kathy, Yau, Shu C, Berg, Jonathan, Ogilvie, Caroline Mackie
Published in BioTechniques (01.09.2004)
Published in BioTechniques (01.09.2004)
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A novel and rapid mutation screening approach facilitates prenatal diagnosis
Ashton, Emma, Deans, Zandra, Yau, Shu C., Abbs, Stephen
Published in Prenatal diagnosis (01.05.2005)
Published in Prenatal diagnosis (01.05.2005)
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Low prevalence of BRCA1 exon rearrangements in familial and young sporadic breast cancer patients
Ellis, David, Patel, Yogen, Yau, Shu C, Hodgson, Shirley V, Abbs, Stephen J
Published in Familial cancer (01.11.2006)
Published in Familial cancer (01.11.2006)
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Marked Hemiatrophy in Carriers of Duchenne Muscular Dystrophy
Rajakulendran, Sanjeev, Kuntzer, Thierry, Dunand, Murielle, Yau, Shu C, Ashton, Emma J, Storey, Helen, McCauley, Joanna, Abbs, Stephen, Thonney, Francine, Leturcq, France, Lobrinus, Johannes A, Yousry, Tarek, Farmer, Simon, Holton, Janice L, Hanna, Michael G
Published in Archives of neurology (Chicago) (01.04.2010)
Published in Archives of neurology (Chicago) (01.04.2010)
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A small intraexonic deletion within the dystrophin gene suggests a possible mechanism of mutagenesis
ROBINSON, D. O, BUNYAN, D. J, GABB, H. A, TEMPLE, I. K, YAU, S. C
Published in Human genetics (01.05.1997)
Published in Human genetics (01.05.1997)
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Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy
Yau, S.C., Roberts, R.G., Bobrow, M., Mathew, C.G.
Published in The Lancet (British edition) (30.01.1993)
Published in The Lancet (British edition) (30.01.1993)
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