Recent Synchronous Radiation of a Living Fossil
Nagalingum, N. S., Marshall, C. R., Quental, T. B., Rai, H. S., Little, D. P., Mathews, S.
Published in Science (American Association for the Advancement of Science) (11.11.2011)
Published in Science (American Association for the Advancement of Science) (11.11.2011)
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Journal Article
Narrative skills in deaf children who use spoken English: Dissociations between macro and microstructural devices
Jones, -->A.C., Toscano, E., Botting, N., Marshall, C.-->R., Atkinson, J.R., Denmark, T., Herman, -->R., Morgan, G.
Published in Research in developmental disabilities (01.12.2016)
Published in Research in developmental disabilities (01.12.2016)
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Journal Article
Effects of Sampling Standardization on Estimates of Phanerozoic Marine Diversification
Alroy, J., Marshall, C. R., Bambach, R. K., Bezusko, K., Foote, M., Fürsich, F. T., Hansen, T. A., Holland, S. M., Ivany, L. C., Jablonski, D., Jacobs, D. K., Jones, D. C., Kosnik, M. A., Lidgard, S., Low, S., Miller, A. I., Novack-Gottshall, P. M., Olszewski, T. D., Patzkowsky, M. E., Raup, D. M., Roy, K., Sepkoski, J. J., Sommers, M. G., Wagner, P. J., Webber, A.
Published in Proceedings of the National Academy of Sciences - PNAS (22.05.2001)
Published in Proceedings of the National Academy of Sciences - PNAS (22.05.2001)
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Journal Article
Hemizygous deletions on chromosome 1p21.3 involving the DPYD gene in individuals with autism spectrum disorder
Carter, MT, Nikkel, SM, Fernandez, BA, Marshall, CR, Noor, A, Lionel, AC, Prasad, A, Pinto, D, Joseph-George, AM, Noakes, C, Fairbrother-Davies, C, Roberts, W, Vincent, J, Weksberg, R, Scherer, SW
Published in Clinical genetics (01.11.2011)
Published in Clinical genetics (01.11.2011)
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Journal Article
The Link between Prosody and Language Skills in Children with Specific Language Impairment (SLI) and/or Dyslexia
Marshall, C. R, Harcourt-Brown, S, Ramus, F, van der Lely, H. K. J
Published in International journal of language & communication disorders (01.07.2009)
Published in International journal of language & communication disorders (01.07.2009)
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Journal Article
Asymmetrical attenuation of vibration sensation in unilateral diabetic Charcot foot neuroarthropathy
Valabhji, J., Marshall, R. C., Lyons, S., Bloomfield, L., Hogg, D., Rosenfeld, P., Gabriel, C. M.
Published in Diabetic medicine (01.09.2012)
Published in Diabetic medicine (01.09.2012)
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Journal Article
Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathy
Peña‐Padilla, C., Marshall, C.R., Walker, S., Scherer, S.W., Tavares‐Macías, G., Razo‐Jiménez, G., Bobadilla‐Morales, L., Acosta‐Fernández, E., Corona‐Rivera, A., Mendoza‐Londono, R., Corona‐Rivera, J. R.
Published in Clinical genetics (01.04.2017)
Published in Clinical genetics (01.04.2017)
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Journal Article
Mapping of three novel loci for non-syndromic autosomal recessive mental retardation (NS-ARMR) in consanguineous families from Pakistan
Rafiq, MA, Ansar, M, Marshall, CR, Noor, A, Shaheen, N, Mowjoodi, A, Khan, MA, Ali, G, Amin-ud-Din, M, Feuk, L, Vincent, JB, Scherer, SW
Published in Clinical genetics (01.11.2010)
Published in Clinical genetics (01.11.2010)
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Journal Article
The effect of dyslexia on information retrieval A pilot study
MACFARLANE, A, AL-WABIL, A, MARSHALL, C. R, ALBRAIR, A, JONES, S. A, ZAPHIRIS, P
Published in Journal of documentation (27.04.2010)
Published in Journal of documentation (27.04.2010)
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Journal Article
On the role of transverse motion in pseudo-steady gravity currents
Marshall, C. R., Dorrell, R. M., Keevil, G. M., Peakall, J., Tobias, S. M.
Published in Experiments in fluids (01.03.2023)
Published in Experiments in fluids (01.03.2023)
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Journal Article
Observations of large-scale coherent structures in gravity currents: implications for flow dynamics
Marshall, C. R., Dorrell, R. M., Keevil, G. M., Peakall, J., Tobias, S. M.
Published in Experiments in fluids (01.06.2021)
Published in Experiments in fluids (01.06.2021)
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Journal Article
Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays
Costain, Gregory, Lionel, Anath C, Merico, Daniele, Forsythe, Pamela, Russell, Kathryn, Lowther, Chelsea, Yuen, Tracy, Husted, Janice, Stavropoulos, Dimitri J, Speevak, Marsha, Chow, Eva W C, Marshall, Christian R, Scherer, Stephen W, Bassett, Anne S
Published in Human molecular genetics (15.11.2013)
Published in Human molecular genetics (15.11.2013)
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Journal Article
Mutations of c-kit JM domain are found in a minority of human gastrointestinal stromal tumors
MOSKALUK, C. A, TIAN, Q, MARSHALL, C. R, RUMPEL, C. A, FRANQUEMONT, D. W, FRIERSON, H. F
Published in Oncogene (11.03.1999)
Published in Oncogene (11.03.1999)
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Journal Article
Quantifying the dark data in museum fossil collections as palaeontology undergoes a second digital revolution
Marshall, C. R., Finnegan, S., Clites, E. C., Holroyd, P. A., Bonuso, N., Cortez, C., Davis, E., Dietl, G. P., Druckenmiller, P. S., Eng, R. C., Garcia, C., Estes-Smargiassi, K., Hendy, A., Hollis, K. A., Little, H., Nesbitt, E. A., Roopnarine, P., Skibinski, L., Vendetti, J., White, L. D.
Published in Biology letters (2005) (01.09.2018)
Published in Biology letters (2005) (01.09.2018)
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Journal Article
Painful exostosis of the external occipital protuberance
Marshall, R.C, Abela, C, Eccles, S
Published in Journal of plastic, reconstructive & aesthetic surgery (01.11.2015)
Published in Journal of plastic, reconstructive & aesthetic surgery (01.11.2015)
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Journal Article
Phenotypic spectrum associated with PTCHD1 deletions and truncating mutations includes intellectual disability and autism spectrum disorder
Chaudhry, A., Noor, A., Degagne, B., Baker, K., Bok, L. A., Brady, A. F., Chitayat, D., Chung, B. H., Cytrynbaum, C., Dyment, D., Filges, I., Helm, B., Hutchison, H. T., Jeng, L. J. B., Laumonnier, F., Marshall, C. R., Menzel, M., Parkash, S., Parker, M. J., Raymond, L. F., Rideout, A. L., Roberts, W., Rupps, R., Schanze, I., Schrander-Stumpel, C. T. R. M., Speevak, M. D., Stavropoulos, D. J., Stevens, S. J. C., Thomas, E. R. A., Toutain, A., Vergano, S., Weksberg, R., Scherer, S. W., Vincent, J. B., Carter, M. T.
Published in Clinical genetics (01.09.2015)
Published in Clinical genetics (01.09.2015)
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Journal Article