Down syndrome: National conference on patient registries, research databases, and biobanks

A December 2010 meeting, “Down Syndrome: National Conference on Patient Registries, Research Databases, and Biobanks,” was jointly sponsored by the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) at the National Institutes of Health (NIH) in Bethesda, MD, and...

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Veröffentlicht in:	Molecular genetics and metabolism 2011-09, Vol.104 (1-2), p.13-22
Hauptverfasser:	Oster-Granite, Mary Lou, Parisi, Melissa A., Abbeduto, Leonard, Berlin, Dorit S., Bodine, Cathy, Bynum, Dana, Capone, George, Collier, Elaine, Hall, Dan, Kaeser, Lisa, Kaufmann, Petra, Krischer, Jeffrey, Livingston, Michelle, McCabe, Linda L., Pace, Jill, Pfenninger, Karl, Rasmussen, Sonja A., Reeves, Roger H., Rubinstein, Yaffa, Sherman, Stephanie, Terry, Sharon F., SieWhitten, Michelle, Williams, Stephen, McCabe, Edward R.B., Maddox, Yvonne T.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biobank Biological Specimen Banks - statistics & numerical data Biomedical Research - statistics & numerical data Databases as Topic - statistics & numerical data Down syndrome Down Syndrome - epidemiology Humans Registries - statistics & numerical data Registry Trisomy 21 United States - epidemiology
Online-Zugang:	Volltext
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