Life expectancy and death from cardiomyopathy amongst carriers of Duchenne and Becker muscular dystrophy in Scotland von Holloway, S M, Wilcox, D E, Wilcox, A, Dean, J C S, Berg, J N, Goudie, D R, Denvir, M A, Porteous, M E M

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Long term health and neurodevelopment in children exposed to antiepileptic drugs before birth von Dean, J C S, Hailey, H, Moore, S J, Lloyd, D J, Turnpenny, P D, Little, J

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ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency von Olsen, Rikke K. J., Olpin, Simon E., Andresen, Brage S., Miedzybrodzka, Zofia H., Pourfarzam, Morteza, Merinero, Begoña, Frerman, Frank E., Beresford, Michael W., Dean, John C. S., Cornelius, Nanna, Andersen, Oluf, Oldfors, Anders, Holme, Elisabeth, Gregersen, Niels, Turnbull, Douglass M., Morris, Andrew A. M.

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Phenotypic spectrum associated with de novo mutations in QRICH1 gene von Ververi, A., Splitt, M., Dean, J. C. S., Brady, A. F.

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Phenotype‐driven molecular autopsy for sudden cardiac death von Cann, F., Corbett, M., O'Sullivan, D., Tennant, S., Hailey, H., Grieve, J.H.K., Broadhurst, P., Rankin, R., Dean, J.C.S.

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A clinical study of 57 children with fetal anticonvulsant syndromes von Moore, S J, Turnpenny, P, Quinn, A, Glover, S, Lloyd, D J, Montgomery, T, Dean, J C S

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A high frequency of the MTHFR 677C>T polymorphism in Scottish women with epilepsy: Possible role in pathogenesis von Dean, J.C.S, Robertson, Z, Reid, V, Wang, Q, Hailey, H, Moore, S, Rasalam, A.D, Turnpenny, P, Lloyd, D, Shaw, D, Little, J

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Characteristics of fetal anticonvulsant syndrome associated autistic disorder von Rasalam, AD, Hailey, H, Williams, JHG, Moore, SJ, Turnpenny, PD, Lloyd, DJ, Dean, JCS

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Fragile X syndrome with FMR1 and FMR2 deletion von Moore, S J, Strain, L, Cole, G F, Miedzybrodzka, Z, Kelly, K F, Dean, J C S

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Characteristics of fetal anticonvulsant syndrome associated autistic disorder von Rasalam, AD, Hailey, H, Williams, J H G, Moore, S J, Turnpenny, P D, Lloyd, D J, Dean, J C S

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Management of Marfan syndrome von Dean, John C S

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Chromosome 22q11 microdeletion and congenital heart disease--a survey in a paediatric population von Yong, D E, Booth, P, Baruni, J, Massie, D, Stephen, G, Couzin, D, Dean, J C

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Protrusio acetabuli in Marfan's syndrome von Yule, S.R., Hobson, E.E., Dean, J.C.S., Gilbert, F.J.

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A Clinical Study of 57 Children With Fetal Anticonvulsant Syndromes von Moore, S. J, Turnpenny, P, Quinn, A, Glover, S, Lloyd, D. J, Montgomery, T, Dean, J. C. S

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Catalog of Teratogenic Agents: 10th edition. Thomas H Shepard. Baltimore: The Johns Hopkins University Press. 2001. ISBN 0-8018-6722-3 von Dean, J. C S

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A True Hermaphrodite Chimera Resulting from Embryo Amalgamation after in Vitro Fertilization von Strain, Lisa, Dean, John C.S, Hamilton, Mark P.R, Bonthron, David T

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Type III collagen mutations cause fragile cerebral arteries von Pope, F. M., Kendall, B. E., Slapak, G. I., Kapoor, R., McDonald, W. I., Compston, D. A. S., Mitchell, R., Hope, D. T., Millar-Craig, M. W., Dean, J. C. S., Johnston, A. W., Lynch, P. G., Sarathchandra, P., Narcisi, P., Nicholls, A. C., Richards, A. J., Mackenzie, J. L.

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Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene von Dean, John Cs, Moore, Susan J, Osborne, Aileen, Howe, Jonathan, Turnpenny, Peter D

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Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis von Reardon, W, Wilkes, D, Rutland, P, Pulleyn, L J, Malcolm, S, Dean, J C, Evans, R D, Jones, B M, Hayward, R, Hall, C M, Nevin, N C, Baraister, M, Winter, R M

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Life expectancy in British Marfan syndrome populations von Gray, JR, Bridges, AB, West, RR, McLeish, L., Stuart, AG, Dean, JCS, Porteous, MEM, Boxer, M., Davies, SJ

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