Embryonic development and pattern formation
Morriss-Kay, G.M. (Department of Human Anatomy, Oxford, UK.), Sokolova, N
Published in The FASEB journal (01.07.1996)
Published in The FASEB journal (01.07.1996)
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Journal Article
Development and tissue origins of the mammalian cranial base
McBratney-Owen, B., Iseki, S., Bamforth, S.D., Olsen, B.R., Morriss-Kay, G.M.
Published in Developmental biology (01.10.2008)
Published in Developmental biology (01.10.2008)
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De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome
Oldridge, Michael, Zackai, Elaine H., McDonald-McGinn, Donna M., Iseki, Sachiko, Morriss-Kay, Gillian M., Twigg, Stephen R.F., Johnson, David, Wall, Steven A., Jiang, Wen, Theda, Christiane, Jabs, Ethylin Wang, Wilkie, Andrew O.M.
Published in American journal of human genetics (01.02.1999)
Published in American journal of human genetics (01.02.1999)
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Analysis of limb reduction defects in babies exposed to chorionic villus sampling
Firth, H.V., Huson, S.M., Boyd, P.A., Chamberlain, P.F., MacKenzie, Iz, Morriss-Kay, G.M.
Published in The Lancet (British edition) (30.04.1994)
Published in The Lancet (British edition) (30.04.1994)
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Mutations of Ephrin-B1 (EFNB1), a Marker of Tissue Boundary Formation, Cause Craniofrontonasal Syndrome
Stephen R. F. Twigg, Kan, Rui, Babbs, Christian, Bochukova, Elena G., Robertson, Stephen P., Wall, Steven A., Morriss-Kay, Gillian M., Andrew O. M. Wilkie, Weatherall, David
Published in Proceedings of the National Academy of Sciences - PNAS (08.06.2004)
Published in Proceedings of the National Academy of Sciences - PNAS (08.06.2004)
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Differential effects of FGFR2 mutations on syndactyly and cleft palate in Apert syndrome
SLANEY, S. F, OLDRIDGE, M, HURST, J. A, MORRISS-KAY, G. M, HALL, C. M, POOLE, M. D, WILKIE, A. O. M
Published in American journal of human genetics (01.05.1996)
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Published in American journal of human genetics (01.05.1996)
Journal Article
Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects
Wilkie, Andrew O.M, Wall, Steven A, Sugayama, Sofia M, Salamanca, Alberto, Kutílek, Stepán, Mavrogiannis, Lampros A, Baxová, Alica, Morriss-Kay, Gillian M, Antonopoulou, Ileana, Kim, Chong A
Published in Nature genetics (01.01.2001)
Published in Nature genetics (01.01.2001)
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