Proceedings from the Turner Resource Network symposium: The crossroads of health care research and health care delivery

Turner syndrome, a congenital condition that affects ∼1/2,500 births, results from absence or structural alteration of the second sex chromosome. There has been substantial effort by numerous clinical and genetic research groups to delineate the clinical, pathophysiological, cytogenetic, and molecul...

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Veröffentlicht in:	American journal of medical genetics. Part A 2015-09, Vol.167A (9), p.1962-1971
Hauptverfasser:	Backeljauw, Philippe F., Bondy, Carolyn, Chernausek, Steven D., Cernich, Joseph T., Cole, David A., Fasciano, Laura P., Foodim, Joan, Hawley, Scott, Hong, David S., Knickmeyer, Rebecca C., Kruszka, Paul, Lin, Angela E., Lippe, Barbara M., Lorigan, Gary A., Maslen, Cheryl L., Mauras, Nelly, Page, David C., Pemberton, Victoria L., Prakash, Siddharth K., Quigley, Charmian A., Ranallo, Kelly C., Reiss, Allan L., Sandberg, David E., Scurlock, Cindy, Silberbach, Michael
Format:	Artikel
Sprache:	eng
Schlagworte:	chromosome congenital heart disease Delivery of Health Care - methods Female Genetic Research genetics Health Services Research - methods Humans monosomy X neurodevelopment quality of life Registries sex chromosomes Sex Chromosomes - genetics Turner syndrome Turner Syndrome - genetics women women's health
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