Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis
Chudley, Albert E, Conry, Julianne, Cook, Jocelynn L, Loock, Christine, Rosales, Ted, LeBlanc, Nicole
Published in Canadian Medical Association journal (CMAJ) (01.03.2005)
Published in Canadian Medical Association journal (CMAJ) (01.03.2005)
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Homozygous Deletion of the Very Low Density Lipoprotein Receptor Gene Causes Autosomal Recessive Cerebellar Hypoplasia with Cerebral Gyral Simplification
Boycott, Kym M., Flavelle, Shauna, Bureau, Alexandre, Glass, Hannah C., Fujiwara, T. Mary, Wirrell, Elaine, Davey, Krista, Chudley, Albert E., Scott, James N., McLeod, D. Ross, Parboosingh, Jillian S.
Published in American journal of human genetics (01.09.2005)
Published in American journal of human genetics (01.09.2005)
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Fetal alcohol spectrum disorder
Koren, Gideon, Nulman, Irena, Chudley, Albert E, Loocke, Christine
Published in Canadian Medical Association journal (CMAJ) (25.11.2003)
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Published in Canadian Medical Association journal (CMAJ) (25.11.2003)
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Evaluation of spatial working memory function in children and adults with fetal alcohol spectrum disorders: a functional magnetic resonance imaging study
Malisza, Krisztina L, Allman, Ava-Ann, Shiloff, Deborah, Jakobson, Lorna, Longstaffe, Sally, Chudley, Albert E
Published in Pediatric research (01.12.2005)
Published in Pediatric research (01.12.2005)
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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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Identifying fetal alcohol spectrum disorder in primary care
Loock, Christine, Conry, Julianne, Cook, Jocelynn L, Chudley, Albert E, Rosales, Ted
Published in Canadian Medical Association journal (CMAJ) (01.03.2005)
Published in Canadian Medical Association journal (CMAJ) (01.03.2005)
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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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Subtelomeric deletions of chromosome 6p: Molecular and cytogenetic characterization of three new cases with phenotypic overlap with Ritscher-Schinzel (3C) syndrome
DeScipio, Cheryl, Schneider, Lori, Young, Terri L., Wasserman, Nora, Yaeger, Dinah, Lu, Fengmin, Wheeler, Patricia G., Williams, Marc S., Bason, Lynn, Jukofsky, Lori, Menon, Ammini, Geschwindt, Ryan, Chudley, Albert E., Saraiva, Jorge, Schinzel, Albert A. G. L., Guichet, Agnes, Dobyns, William E., Toutain, Annick, Spinner, Nancy B., Krantz, Ian D.
Published in American journal of medical genetics. Part A (01.04.2005)
Published in American journal of medical genetics. Part A (01.04.2005)
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Mutation in the 5' alternatively spliced region of the XNP/ATR-X gene causes Chudley-Lowry syndrome
Abidi, Fatima E, Cardoso, Carlos, Lossi, Anne-Marie, Lowry, Robert Brian, Depetris, Danielle, Mattéi, Marie-Geneviève, Lubs, Herbert A, Stevenson, Roger E, Fontes, Michel, Chudley, Albert E, Schwartz, Charles E
Published in European journal of human genetics : EJHG (01.02.2005)
Published in European journal of human genetics : EJHG (01.02.2005)
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Journal Article
autosomal recessive cerebellar hypoplasia in the hutterite population
glass, hannah c, boycott, kym m, adams, coleen, barlow, karen, scott, james n, chudley, albert e, fujiwara, t mary, morgan, kenneth, wirrell, elaine, mcleod, d ross
Published in Developmental medicine and child neurology (01.10.2005)
Published in Developmental medicine and child neurology (01.10.2005)
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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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