The copy number variant involving part of the α7 nicotinic receptor gene contains a polymorphic inversion von Flomen, Rachel H, Davies, Angela F, Di Forti, Marta, Cascia, Caterina La, Mackie-Ogilvie, Caroline, Murray, Robin, Makoff, Andrew J

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Meiotic outcomes of three-way translocations ascertained in cleavage-stage embryos: refinement of reproductive risks and implications for PGD von Scriven, Paul N, Bint, Susan M, Davies, Angela F, Ogilvie, Caroline Mackie

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Long-term episomal transgene expression from mitotically stable integration-deficient lentiviral vectors von Kymäläinen, Hanna, Appelt, J Uwe, Giordano, Frank A, Davies, Angela F, Ogilvie, Caroline M, Ahmed, Sherif G, Laufs, Stephanie, Schmidt, Manfred, Bode, Juergen, Yáñez-Muñoz, Rafael J, Dickson, George

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Multicolor banding remains an important adjunct to array CGH and conventional karyotyping von Bint, Susan M, Davies, Angela F, Ogilvie, Caroline Mackie

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Separation of the PROX1 gene from upstream conserved elements in a complex inversion/translocation patient with hypoplastic left heart von Gill, Harinder K, Parsons, Sian R, Spalluto, Cosma, Davies, Angela F, Knorz, Victoria J, Burlinson, Clare EG, Ng, Bee Ling, Carter, Nigel P, Ogilvie, Caroline Mackie, Wilson, David I, Roberts, Roland G

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Delineation of two distinct 6p deletion syndromes von DAVIES, A. F, MIRZA, G, RAGOUSSIS, J, SEKHON, G, TURNPENNY, P, LEROY, F, SPELEMAN, F, LAW, C, VAN REGEMORTER, N, VAMOS, E, FLINTER, F

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Prevalence of Angelman syndrome amongst referrals with epilepsy and developmental delay von Davies, Angela F., Ogilvie, Caroline Mackie

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Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation von Behjati, Farkhondeh, Shafeghati, Yousef, Kahrizi, Kimia, Firouzabadi, Saghar Ghasemi, Najmabadi, Hossein, Dixon, Neil, Davies, Angela F.

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Characterization of terminal chromosome anomalies using multisubtelomere FISH von Davies, Angela F., Kirby, Toby L., Docherty, Zoe, Mackie Ogilvie, Caroline

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Isolation and chromosomal mapping of human glycogen synthase kinase-3 α and -3 β encoding genes von Shaw, Pang-Chui, Davies, Angela F, Lau, Kwok-Fai, Garcia-Barcelo, Merce, Waye, Mary MY, Lovestone, Simon, Miller, Christopher CJ, Anderton, Brian H

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Physical map of human 6p21.2-6p21.3: region flanking the centromeric end of the major histocompatibility complex von Tripodis, N, Mason, R, Humphray, S J, Davies, A F, Herberg, J A, Trowsdale, J, Nizetic, D, Senger, G, Ragoussis, J

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A detailed investigation of two cases exhibiting characteristics of the 6p deletion syndrome von Davies, A F, Olavesen, M G, Stephens, R J, Davidson, R, Delneste, D, Van Regemorter, N, Vamos, E, Flinter, F, Abusaad, I, Ragoussis, J

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The copy number variant involving part of the alpha7 nicotinic receptor gene contains a polymorphic inversion von Flomen, Rachel H, Davies, Angela F, Di Forti, Marta, La Cascia, Caterina, Mackie-Ogilvie, Caroline, Murray, Robin, Makoff, Andrew J

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Rapid molecular method for prenatal detection of Down's syndrome von Pertl, B., Yau, S.C., Sherlock, J., Davies, A., Mathew, C.G., Adinolfi, M.

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An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2α that affects anterior eye chamber development von DAVIES, A. F, MIRZA, G, FLINTER, F, RAGOUSSIS, J

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The copy number variant involving part of the [alpha]7 nicotinic receptor gene contains a polymorphic inversion von Flomen, Rachel H, Davies, Angela F, Di Forti, Marta, Cascia, Caterina La, Mackie-ogilvie, Caroline, Murray, Robin, Makoff, Andrew J

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The copy number variant involving part of the a7 nicotinic receptor gene contains a polymorphic inversion von FLOMEN, Rachel H, DAVIES, Angela F, DI FORTI, Marta, LA CASCIA, Caterina, MACKIE-OGILVIE, Caroline, MURRAY, Robin, MAKOFF, Andrew J

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Isolation and chromosomal mapping of human glycogen synthase kinase-3 α and -3β encoding genes von Shaw, Pang-Chui, Davies, Angela F., Lau, Kwok-Fai, Garcia-Barcelo, Merce, Waye, Mary M.Y., Lovestone, Simon, Miller, Christopher C.J., Anderton, Brian H.

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An interstitial deletion of 6p24-p25 proximal to theFKHL7 locus and includingAP-2α that affects anterior eye chamber development von Davies, Angela F, Mirza, Ghazala, Flinter, Frances, Ragoussis, Jiannis

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An interstitial deletion of 6p24-p25 proximal to theFKHL7 locus and includingAP-2[alpha] that affects anterior eye chamber development von Davies, Angela F, Mirza, Ghazala, Flinter, Frances, Ragoussis, Jiannis

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