Page 241 - ASHG 2013 Program Guide

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POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
2844
T First live birth in Hong Kong after
preimplantation genetic diagnosis on a disease-
predisposition mutation carrier with a novel genomic
deletion in
BRCA2
.
Q. Wang, J. Chow, W. Yeung, E. Lau,
V. Lee, E. Ng, P. C. Ho.
2845
W Embryo SNP array genotyping: A model for
preimplantation diagnosis in human.
F. Campagnari, Y.
T. Utsunomiya, A. S. Carmo, J. A. Vinsintin, J. F. Garcia, C.
Rosenberg, R. V. Alonso.
2846
T KaryoLite® — A rapid single cell screening
assay to simultaneously detect aneuploidies for all
chromosomes from whole-genome amplified DNA
from 3 day blastomeres.
S. Dallaire, R. Walker, M.
Schermer.
2847
W Quebec perspectives on the medical and social
uses of preimplantation genetic diagnosis and on
the current service deliveries.
F. Duplain-Laferrière, R.
Drouin, C. Bouffard.
2848
T
Notchless
impacts multiple signaling pathways
during pre-implantation development.
C.-L. Lo, A. C.
Lossie, J. B. Sherrill.
2849
W The first eport of a viable, 35-week gestation
pregnancy following the transfer of a genetically
normalized blastocyst: Embryo normalization can
occur during differentiation to the blastocyst stage.
W.
G. Kearns, M. St. Amant, B. Welch, J. Carter, A. Potts, P.
R. Brezina, A. T. Benner, K. J. Tobler, G. R. Cutting, R. P.
Dickey.
2850
T Stability testing of a noninvasive prenatal test in
a clinical setting — The MaterniT21™ PLUS laboratory-
developed test.
R. C. Tim, J. A. Tynan, T. J. Jensen, L.
Cagasan, V. Lu, L. Liu, S. Sovath, M. Riviere, P. Oeth, M.
Ehrich.
2851
W Identification of pathogenic CNV by arrayCGH
in prenatal cases with oral clefts.
Y. Cao, Z. Li, J.
Rosenfeld, A. Patel, J. Huang, X. Sun, T. Y. Leung, S. W.
Cheung, K. W. Choy.
2852
T Assessing the utilization and distribution
of an evidence-based resource recommended in
the 2013 American College of Medical Genetics
and Genomics statement on noninvasive prenatal
screening for fetal aneuploidy.
S. Meredith,
B. Skotko, C. Brasington.
2853
W Exploring placental gene expression pattern in
abnormal fetal growth.
A. Sabri, C. H. M. Ng, D. Lai, A.
D’Silva, J. Kaur, J. A. Hyett.
2854
T Diagnostic dilemma: Fetal cardiomyopathy
presenting at a late gestational age.
B. Suskin, K. Bajaj,
M. Rosner, P. Dar, S. Klugman.
2855
W Improving efficiency and cost of next
generation sequencing of maternal cell free DNA for
the detection of fetal aneuploidy.
L. Chitty, J. Weir, C.
Boustred, S. Fielding, F. McKay, H. White, Z. Kingsbury, S.
Humphray, E. Tsogka, N. Lench, J. Betley.
2831
W Gene-environment interaction in adverse
reproductive outcomes.
B. D. Banerjee.
2832
T Trans-ethnic GWAS of pelvic organ
prolapse among African American and Hispanic
postmenopausal women of the Women’s Health
Initiative.
D. R. Velez Edwards, R. M. Ward, A. Giri, K. E.
Hartmann, A. J. Park, C. L. Avery, R. Wallace, G. Bareh, L.
Qi, M. J. O’Sullivan, A. Reiner, T. L. Edwards, J. M. Wu.
2833
W The genetic predisposition for uterine
leiomyomas in recently admixed populations:
A preliminary study in individuals from electronic
medical records.
J. Jeff, G. Belbin, D. Ruderfer, E. Stahl,
S. Purcell, E. Bottinger, R. Loos, O. Gottesman, E. Kenny.
2834
T Role of
Shigella
in etiology of endometriosis.
M. Latha, V. Kutala, Q. Hasan, V. Kodati.
2835
W Identification of di ferentially expressed non-
peptide metabolomic molecules with metabolomics
approach in pregnancy-induced hypertension
syndrome.
X.-C. Luo, J. Pan, X.-G. Tao, X.-L. Zhao, Y. Gu,
Q.-X. Shi, N. Zhong.
2836
T Admixture mapping study of uterine fib oids
finds evidence for fi onectin and diabetes genes.
K. S.
Tsosie, D. R. Velez Edwards, T. L. Edwards.
2837
W The Kallmann syndrome gene
WDR11
and
binding partner EMX1 are expressed in hypothalamic
and gonadal tissues.
E. K. Ko, S. D. Quaynor, L. P. Chorich,
H. G. Kim, S. H. Kim, R. S. Cameron, L. C. Layman.
2838
T Understanding the genetics of spermatogenic
failure by resequencing the sex chromosomes of
infertile men.
R. George, J. Hughes, L. Brown, L. Lin,
D. Koboldt, R. Fulton, R. Wilson, R. Oates, S. Silber, S.
Repping, D. Page.
2839
W Mutations in the kallikrein related peptidase-3
(
KLK3
)
gene affect semen parameters in Indian men.
N. Gupta, D. V. S. Sudhakar, S. N. Sankhwar, N. Gupta, K.
Thangaraj, S. Rajender.
2840
T Expression quantitative trait (eQTL) mapping
in mid-secretory phase endometrial cells identifies
candidate genes for recurrent early pregnancy loss.
C. L. Kagan, G. Kosova, K. Patterson, M. D. Stephenson,
C. Ober.
2841
W The clinical analysis of relationship between
sperm DNA damage and sperm parameters.
F. Kaplan,
S. Aydos, B. Altinok Zaim, I. Yükselen, Y. Yükselten, A.
Sungurog˘ lu, K. Aydos.
2842
T Quantitative analysis of mixtures by deep
sequencing of HLA gene amplicons using next-
generation systems.
B. N. Hoglund, M. Rastrou, D.
Goodridge, H. A. Erlich, C. L. Holcomb.
2843
W Screening models for early detection of late-
onset preeclampsia with various markers in low-risk
pregnancy population.
H. J. Park, D. H. Cha, S. H. Kim,
S. S. Shim, J. Y. Kim, Y. K. Cho, K. J. Lee.