A-Z Articles Index by First Author's Last Name A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

O'Driscoll M et al. A splicing mutation affecting expression of ataxia-telangiectasia and Rad3-related protein (ATR) results in Seckel syndrome. Nat Genet. 2003 Apr;33(4):497-501

Okamoto I et al. Epigenetic dynamics of imprinted X inactivation during early mouse development. Science. 2004 Jan 30;303(5658):644-9. Epub 2003 Dec 11.

Okumiya T et al. Chemical chaperones improve transport and enhance stability of mutant alpha-glucosidases in glycogen storage disease type II. Mol Genet Metab. 2007 Jan;90(1):49-57. Epub 2006 Nov 13.

Olson LE et al. A chromosome 21 critical region does not cause specific down syndrome phenotypes. Science. 2004 Oct 22; 306 (5696): 687-90.

Ooi SK et al. DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA. Nature. 2007 Aug 9;448(7154):714-7.

Ørstavik KH et al. Another Case of Imprinting Defect in a Girl with Angelman Syndrome Who Was Conceived by Intracytoplasmic Sperm Injection. Am J Hum Genet. 2002 Nov 13; 72:000.