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American Journal of Medical Genetics. Part A|January 22, 2004
Spinocerebellar ataxia type 2 (SCA2) presenting with ophthalmoplegia and developmental delay in infancyPaolo Moretti, Maria Blazo, Leonardo Garcia, et al.
International Review of Psychiatry (Abingdon, England)|June 15, 2007
The role of religious fundamentalism in terrorist violence: a social psychological analysisM Brooke Rogers, Kate M Loewenthal, Christopher Alan Lewis, et al.
Neuroscience Letters|December 10, 2017
Regional brain gray matter changes in adolescents with single ventricle heart diseaseSadhana Singh, Rajesh Kumar, Bhaswati Roy, et al.
Psychological Reports|April 4, 2003
Psychological type and attitude toward Christianity: a replicationLeslie J Francis, Mandy Robbins, Anna Boxer, et al.
Molecular Vision|April 10, 2007
Identification of three novel NHS mutations in families with Nance-Horan syndromeKristen M Huang, Junhua Wu, Simon P Brooks, et al.
Ophthalmic Genetics|July 17, 2004
Cytochrome P4501B1 mutations cause only part of primary congenital glaucoma in EcuadorStacey M Curry, Aline G Daou, Pia Hermanns, et al.
American Journal of Medical Genetics. Part A|April 6, 2011
SMAD4 mutation segregating in a family with juvenile polyposis, aortopathy, and mitral valve dysfunctionSara Andrabi, Mir Reza Bekheirnia, Patricia Robbins-Furman, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 14, 2003
Visual loss in patients with cytomegalovirus retinitis and acquired immunodeficiency syndrome before widespread availability of highly active antiretroviral therapyJanet T Holbrook, Douglas A Jabs, David V Weinberg, et al.
American Journal of Human Genetics|February 5, 2003
Identification of a novel Bardet-Biedl syndrome protein, BBS7, that shares structural features with BBS1 and BBS2José L Badano, Stephen J Ansley, Carmen C Leitch, et al.
The Journal of Biological Chemistry|May 6, 2003
NEDP1, a highly conserved cysteine protease that deNEDDylates CullinsHeidi M Mendoza, Lin-Nan Shen, Catherine Botting, et al.
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