Page 197 - ASHG 2012 Annual Meeting Program Guide

186
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
1861
F Alignment and assessment problems in the
undergraduate genetics curriculum.
M. Dougherty,
T. McElhinny, B. Bowling, J. Libarkin.
1862
F YouTube as an educational resource for visual
and kinesthetic learners: A study of DNA replication
animations.
J. M. Lind.
1863
F Genetic counseling in India: Current certification
courses and a need for the development of a master’s
training program.
K. Shah.
Health Services Research
1864
F A strategy of applying comprehensive
therapeutic approaches for training children with
autism.
H. Xu, N. Zhong.
1865
F Genetics and public health: The experience
of a referral center for diagnosis of 22q11.2 deletion
in Brazil and suggestions for implementing genetic
testing.
T. Vieira, I. Sgardioli, V. Gil-da-Silva-Lopes.
1866
F Outreach, genetic counseling and testing of
patients at risk for hereditary breast and ovarian
cancer ascertained through the use of the electronic
medical record.
H. Kershberg, E. Parkhurst, M. Alvarado,
H. Zhou, J. Natoli, G. Tiller.
1867
F Prevalence of Down syndrome in the United
States.
A. P. Presson, G. Partyka, K. M. Jensen, S. A.
Rasmussen, O. J. Devine, L. McCabe, E. R. B. McCabe.
1868
F Rare disease initiatives in Europe: Centers
of expertise in Germany.
C. Huebner, M. Stuhrmann-
Spangenberg, C. Zeidler, J. Schmidtke.
1869
F Implementation of universal Lynch syndrome
screening in an integrated health-care delivery system.
K. A. B. Goddard, T. Kauffman, M. Morse, J. Davis, C.
Young, E. Esterberg, C. McGinley, J. Reiss.
1870
F Beyond NGS technology: Overcoming key
challenges for nation-wide implementation of next-
generation sequencing into routine diagnostics.
T. Vrijenhoek on behalf of Centre for Genome Diagnostics.
1871
F Inherited Neuropathies Consortium: A
collaborative approach to genetic research in
Charcot-Marie-Tooth disease.
F. Speziani, S. M. E.
Feely, C. Siskind, S. H. Blanton, G. Beecham, J. M. Vance,
M. Shy, S. Zuchner, Inherited Neuropathies Consortium.
1872
F Genomic technologies: Effective integration
into pediatric clinical care.
R. Hayeems, N. Hoang, S.
Chenier, J. Stavropoulos, S. Pu, S. Wodak, R. Babul-Hirji,
J. Davies, L. Velsher, J. Aw, R. Weksberg, C. Shuman.
1873
F Genomic technologies: Effective integration
into adult preventive medicine.
N. Hoang, R. Hayeems,
J. Davies, L. Velsher, J. Aw, S. Chenier, J. Stavropoulos,
S. Pu, S. Wodak, R. Babul-Hirji, R. Weksberg, C. Shuman.
science.
D. Murray, D. Whittington, R. Gibbs.
1855
F Pharmacotherapy of Inherited Metabolic
Diseases PharmD Fellowship Training Program.
J. Utz,
W. Whitley.
1856
F Promoting student engagement and critical
thinking in genetics: An evaluation of “Luck of the
Draw” game.
M. Godfrey, A. Bower, K. L. Tracy, R.
Anderson, A. Jameton, B. Arobba, C. Ryan.
1857
F Genetic numeracy in college students:
A quantitative analysis.
M. Bergman, H. Honore Goltz.
1858
F The Growing Stronger Organization and the
Acondroplasia - Achondroplasia Blog: A parents’
initiative to share knowledge and foster alliances
towards potential therapeutic approaches for
achondroplasia.
M. Kaisermann.
1859
F Genetics Home Reference, ten years in: Where
we are now.
S. M. Morrison, M. L. Cheh, S. Calvo, H.
Collins, J. Fun, K. Greenberg, L. Forman-Neall.
1860
F Investigating a conceptual change strategy
to improve student understanding of basic genetics
concepts in undergraduate non-science major and
nursing student populations.
B. Bowling, M. Glassford,
S. Barnes, S. Borgman, E. Reilly, T. Beery, C. Huether.