Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers
Greco, C. M., Hagerman, R. J., Tassone, F., Chudley, A. E., Del Bigio, M. R., Jacquemont, S., Leehey, M., Hagerman, P. J.
Published in Brain (London, England : 1878) (01.08.2002)
Published in Brain (London, England : 1878) (01.08.2002)
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Face-brain asymmetry in autism spectrum disorders
HAMMOND, P, FORSTER-GIBSON, C, CHUDLEY, A. E, ALLANSON, J. E, HUTTON, T. J, FARRELL, S. A, MCKENZIE, J, HOLDEN, J. J. A, LEWIS, M. E. S
Published in Molecular psychiatry (01.06.2008)
Published in Molecular psychiatry (01.06.2008)
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A founder mutation in BBS2 is responsible for Bardet-Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders
Innes, AM, Boycott, KM, Puffenberger, EG, Redl, D, MacDonald, IM, Chudley, AE, Beaulieu, C, Perrier, R, Gillan, T, Wade, A, Parboosingh, JS
Published in Clinical genetics (01.11.2010)
Published in Clinical genetics (01.11.2010)
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Mutations in the Gene for Cardiac Myosin-Binding Protein C and Late-Onset Familial Hypertrophic Cardiomyopathy
Niimura, Hideshi, Bachinski, Linda L, Sangwatanaroj, Somkiat, Watkins, Hugh, Chudley, Albert E, McKenna, William, Kristinsson, Arni, Roberts, Robert, Sole, Michael, Maron, Barry J, Seidman, Christine E, Seidman, J.G, Thierfelder, Ludwig, Jarcho, John A, Anastasakis, Aris, Toutouzas, Pavlos, Elstein, Eleanor, Liew, Choong-Chin, Liew, Jack, Mably, John, Rakowski, Harry, Wigle, E. Douglas, Zhao, Minshun, Salerni, Rosemarie, Bjornsdottir, Halldora
Published in The New England journal of medicine (30.04.1998)
Published in The New England journal of medicine (30.04.1998)
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Mutation analysis of the FRAS1 gene demonstrates new mutations in a propositus with Fraser syndrome
Slavotinek, A., Li, C., Sherr, E.H., Chudley, A.E.
Published in American journal of medical genetics. Part A (15.09.2006)
Published in American journal of medical genetics. Part A (15.09.2006)
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Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features
Dawson, AJ, Putnam, S., Schultz, J., Riordan, D., Prasad, C., Greenberg, CR, Chodirker, BN, Mhanni, AA, Chudley, AE
Published in Clinical genetics (01.12.2002)
Published in Clinical genetics (01.12.2002)
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The Manitoba Youth Justice Program: empowering and supporting youth with FASD in conflict with the law
Longstaffe, S, Chudley, A E, Harvie, M K, Markesteyn, T, Neault, D, Brown, T
Published in Biochemistry and cell biology (01.03.2018)
Published in Biochemistry and cell biology (01.03.2018)
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Molecular cytogenetic investigation of two patients with Y chromosome rearrangements and intellectual disability
Tyson, C., Dawson, A.J., Bal, S., Tomiuk, M., Anderson, T., Tucker, D., Riordan, D., Chudoba, I., Morash, B., Mhanni, A., Chudley, A.E., McGillivray, B., Parslow, M., Rappold, G., Roeth, R., Fawcett, C., Qiao, Y., Harvard, C., Rajcan‐Separovic, E.
Published in American journal of medical genetics. Part A (01.03.2009)
Published in American journal of medical genetics. Part A (01.03.2009)
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Cytogenetic microarrays in Manitoba patients with developmental delay
Dawson, AJ, Riordan, D, Tomiuk, M, Konkin, D, Anderson, T, Bocangel, P, Lwiwiski, N, Saltel-Olson, J, Marles, S, Greenberg, CR, Mhanni, A, Chodirker, BN, Chudley, AE
Published in Clinical genetics (01.05.2009)
Published in Clinical genetics (01.05.2009)
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Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype
Prasad, Chitra, Prasad, Asuri N, Chodirker, Bernard N, Lee, Christine, Dawson, Angelika K, Jocelyn, Leslie J, Chudley, Albert E
Published in Clinical genetics (01.02.2000)
Published in Clinical genetics (01.02.2000)
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Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1
Slavotinek, Anne M, Baranzini, Sergio E, Schanze, Denny, Labelle-Dumais, Cassandre, Short, Kieran M, Chao, Ryan, Yahyavi, Mani, Bijlsma, Emilia K, Chu, Catherine, Musone, Stacey, Wheatley, Ashleigh, Kwok, Pui-Yan, Marles, Sandra, Fryns, Jean-Pierre, Maga, A Murat, Hassan, Mohamed G, Gould, Douglas B, Madireddy, Lohith, Li, Chumei, Cox, Timothy C, Smyth, Ian, Chudley, Albert E, Zenker, Martin
Published in Journal of medical genetics (01.06.2011)
Published in Journal of medical genetics (01.06.2011)
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