From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience.
Genetics in medicine : official journal of the American College of Medical Genetics 2016 Jun .
Lee Elizabeth M J, Xu Karen, Mosbrook Emma, Links Amanda, Guzman Jessica, Adams David R, Flynn Elise, Valkanas Elise, Toro Camillo, Tifft Cynthia J, Boerkoel Cornelius F, Gahl William A, Sincan Mur - Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.
European journal of human genetics : EJHG 2015 Sep .
Srebniak Malgorzata I, Diderich Karin Em, Joosten Marieke, Govaerts Lutgarde Cp, Knijnenburg Jeroen, de Vries Femke At, Boter Marjan, Lont Debora, Knapen Maarten Fcm, de Wit Merel C, Go Attie Tji, Galjaard Robert-Jan H, Van Opstal Dia - Accurate Imputation-Based Screening of Gln368Ter Myocilin Variant in Primary Open-Angle Glaucoma.
Investigative ophthalmology & visual science 2015 Aug 56 (9): 5087-93.
Gharahkhani Puya, Burdon Kathryn P, Hewitt Alex W, Law Matthew H, Souzeau Emmanuelle, Montgomery Grant W, Radford-Smith Graham, Mackey David A, Craig Jamie E, MacGregor Stua - Array CGH as a first-tier test for neonates with congenital heart disease.
Cardiology in the young 2015 Jan 25 (1): 115-22.
Bachman Kristine K, DeWard Stephanie J, Chrysostomou Constantinos, Munoz Ricardo, Madan-Khetarpal Sunee - A protocol for the identification and validation of novel genetic causes of kidney disease.
BMC nephrology 2015 16 (1): 152.
Mallett Andrew, Patel Chirag, Maier Barbara, McGaughran Julie, Gabbett Michael, Takasato Minoru, Cameron Anne, Trnka Peter, I Alexander Stephen, Rangan Gopala, Tchan Michel C, Caruana Georgina, John George, Quinlan Cathy, McCarthy Hugh J, Hyland Valentine, E Hoy Wendy, Wolvetang Ernst, Taft Ryan, Simons Cas, Healy Helen, Little Melis
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