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Proceedings from the Turner Resource Network symposium: The crossroads of health care research and health care delivery
dc.contributor.authorBackeljauw, Philippe F.en_US
dc.contributor.authorBondy, Carolynen_US
dc.contributor.authorChernausek, Steven D.en_US
dc.contributor.authorCernich, Joseph T.en_US
dc.contributor.authorCole, David A.en_US
dc.contributor.authorFasciano, Laura P.en_US
dc.contributor.authorFoodim, Joanen_US
dc.contributor.authorHawley, Scotten_US
dc.contributor.authorHong, David S.en_US
dc.contributor.authorKnickmeyer, Rebecca C.en_US
dc.contributor.authorKruszka, Paulen_US
dc.contributor.authorLin, Angela E.en_US
dc.contributor.authorLippe, Barbara M.en_US
dc.contributor.authorLorigan, Gary A.en_US
dc.contributor.authorMaslen, Cheryl L.en_US
dc.contributor.authorMauras, Nellyen_US
dc.contributor.authorPage, David C.en_US
dc.contributor.authorPemberton, Victoria L.en_US
dc.contributor.authorPrakash, Siddharth K.en_US
dc.contributor.authorQuigley, Charmian A.en_US
dc.contributor.authorRanallo, Kelly C.en_US
dc.contributor.authorReiss, Allan L.en_US
dc.contributor.authorSandberg, David E.en_US
dc.contributor.authorScurlock, Cindyen_US
dc.contributor.authorSilberbach, Michaelen_US
dc.date.accessioned2015-09-01T19:30:32Z
dc.date.available2016-10-10T14:50:23Zen
dc.date.issued2015-09en_US
dc.identifier.citationBackeljauw, 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 (2015). "Proceedings from the Turner Resource Network symposium: The crossroads of health care research and health care delivery." American Journal of Medical Genetics Part A 167(9): 1962-1971.en_US
dc.identifier.issn1552-4825en_US
dc.identifier.issn1552-4833en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/113136
dc.publisherWiley Periodicals, Inc.en_US
dc.subject.othergeneticsen_US
dc.subject.otherchromosomeen_US
dc.subject.othersex chromosomesen_US
dc.subject.otherwomen's healthen_US
dc.subject.otherquality of lifeen_US
dc.subject.othermonosomy Xen_US
dc.subject.otherTurner syndromeen_US
dc.subject.otherwomenen_US
dc.subject.othercongenital heart diseaseen_US
dc.subject.otherneurodevelopmenten_US
dc.titleProceedings from the Turner Resource Network symposium: The crossroads of health care research and health care deliveryen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelGeneticsen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/113136/1/ajmga37121.pdf
dc.identifier.doi10.1002/ajmg.a.37121en_US
dc.identifier.sourceAmerican Journal of Medical Genetics Part Aen_US
dc.identifier.citedreferenceGreen T, Chromik LC, Mazaika PK, Fierro K, Raman MM, Lazzeroni LC, Hong DS, Reiss AL. 2014. Aberrant parietal cortex developmental trajectories in girls with Turner syndrome and related visual‐spatial cognitive development: A preliminary study. Am J Med Genet Part B Neuropsychiatr Genet 165B: 531 – 540.en_US
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dc.identifier.citedreferenceBondy CA, Turner Syndrome Study G. 2007. Care of girls and women with Turner syndrome: A guideline of the Turner Syndrome Study Group. J Clin Endocrinol Metab 92: 10 – 25.en_US
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dc.identifier.citedreferenceAmerican Academy of Pediatrics, American Academy of Family Physicians, American College of Physicians, Transitions Clinical Report Authoring Group 2011. Supporting the Health Care Transition From Adolescence to Adulthood in the Medical Home. 128: 182 – 200.en_US
dc.identifier.citedreferenceAbd‐Elmoniem KZ, Bakalov VK, Matta JR, Muldoon N, Hanover JA, Bondy CA, Gharib AM. 2014. X chromosome parental origin and aortic stiffness in turner syndrome. Clin Endocrinol (Oxf) 81: 467 – 470.en_US
dc.identifier.citedreferenceZinn AR, Page DC, Fisher EM. 1993. Turner syndrome: The case of the missing sex chromosome. Trends Genet 9: 90 – 93.en_US
dc.identifier.citedreferenceWatanabe M, Zinn AR, Page DC, Nishimoto T. 1993. Functional equivalence of human X‐ and Y‐encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome. Nat Genet 4: 268 – 271.en_US
dc.identifier.citedreferenceTorres‐Santiago L, Mericq V, Taboada M, Unanue N, Klein KO, Singh R, Hossain J, Santen RJ, Ross JL, Mauras N. 2013. Metabolic effects of oral versus transdermal 17beta‐estradiol (E(2)): A randomized clinical trial in girls with Turner syndrome. J Clin Endocrinol Metab 98: 2716 – 2724.en_US
dc.identifier.citedreferenceSchoemaker MJ, Swerdlow AJ, Higgins CD, Wright AF, Jacobs PA. 2008. Mortality in women with turner syndrome in Great Britain: A national cohort study. J Clin Endocrinol Metab 93: 4735 – 4742.en_US
dc.identifier.citedreferenceKroner BL, Tolunay HE, Basson CT, Pyeritz RE, Holmes KW, Maslen CL, Milewicz DM, LeMaire SA, Hendershot T, Desvigne‐Nickens P, Devereux RB, Dietz HC, Song HK, Ringer D, Mitchell M, Weinsaft JW, Ravekes W, Menashe V, Eagle KA. 2011. The National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (GenTAC): Results from phase I and scientific opportunities in phase II. Am Heart J 162: 627 – 632.e1.en_US
dc.identifier.citedreferenceKnickmeyer RC. 2012. Turner syndrome: Advances in understanding altered cognition, brain structure, and function. Curr Opin Neurol 25: 144 – 149.en_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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