| Wang Z, McPeek MS
ATRIUM: Testing Untyped SNPs in Case-Control Association Studies with Related Individuals. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):667-78.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Talmud PJ, Drenos F, Shah S, et al.
Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):628-42.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Audo I, Kohl S, Leroy BP, et al.
TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):720-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Zweier C, de Jong EK, Zweier M, et al.
CNTNAP2 and NRXN1 Are Mutated in Autosomal-Recessive Pitt-Hopkins-like Mental Retardation and Determine the Level of a Common Synaptic Protein in Drosophila. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):655-66.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Medland SE, Nyholt DR, Painter JN, et al.
Common variants in the trichohyalin gene are associated with straight hair in europeans. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):750-5.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Abdollahi MR, Morrison E, Sirey T, et al.
Mutation of the Variant alpha-Tubulin TUBA8 Results in Polymicrogyria with Optic Nerve Hypoplasia. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):737-44.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | van Genderen MM, Bijveld MM, Claassen YB, et al.
Mutations in TRPM1 Are a Common Cause of Complete Congenital Stationary Night Blindness. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):730-6.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Li Z, Sergouniotis PI, Michaelides M, et al.
Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):711-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Zhao C, Bellur DL, Lu S, et al.
Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs. [Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't]
Am J Hum Genet 2009 Nov; 85(5):617-27.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kaufman DJ, Murphy-Bollinger J, Scott J, et al.
Public Opinion about the Importance of Privacy in Biobank Research. [Journal Article]
Am J Hum Genet 2009 Nov; 85(5):643-54.
Abstract | Full Citation | Publisher Full Text | Find Related Articles |   |
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