Page 242 - ASHG 2013 Program Guide

POSTER SESSIONS
  229
POSTER SESSIONS
W=W
ednesday authors will present; T=Thursday authors will present; F=Friday authors will pr
esent
2869
W Integrative transcriptome analysis reveals
dysregulation of canonical cancer molecular pathways
in placenta leading to preeclampsia.
R. Moslehi, J. L.
Mills, C. Signore, A. Kumar, X. Ambroggio, A. Dzutsev.
2870
T TLR SNP T399I and early gestational age in
a Wisconsin population of black newborn infants.
D. Pillers, M. Baker, S. Schrodi, L. Zyduck, J. DeValk,
B. Pattnaik, S. Tokarz.
2871
W Copy number variation of
RYR1
locus, which
is involved in myomentrial contraction and relaxation,
is associated with preterm births.
M. Liu, Y. Chen,
N. Zhong.
2872
T LncRNA pathways involved in premature
preterm rupture of membrane.
Q. Shi, X.-C. Luo, Y. Gu,
J. Pan, N. Zhong.
2873
W Functional validation of severe ciliopathies in
a cohort of terminated pregnancies.
F. W. Verheijen,
R. Oegema, L. M. van Unen, J. M. Verhagen, K. M.
Diderich, M. L. van der Sterre, R. M. Hofstra, G. M.
Mancini.
2874
T An inverse association between telomere
lengths and gestational age.
H. Naderi, K. Ryckman,
J. Dagle, J. Murray.
2875
W Case report of a pregnant woman with inherited
thrombocytopenia associated with
MYH9
mutation.
O. Samura, T. Mizunoe, S. Kunishima.
2876
T
KIR2DL4
polymorphism and perinatal HIV-1
transmission.
C. Czarnecki, E. Rossnagel, S. Ramdahin,
J. Embree, F. Plummer, M. Luo.
2877
W Genome-wide association study identifies
more than 10 loci associated with hypospadias.
F.
Geller, B. Feenstra, L. van der Zanden, A. Nordenskjöld,
L. Carstensen, I. van Rooij, I. Baranowska-Körberg,
T. Schnack, M. Melbye.
2878
T Simultaneous uniparental disomy of
chromosome 5 and 16: A case report.
H. Akar, D. Torun,
Y. Tunca.
2879
W Proviral loads of human T-cell leukemia virus
type 1 in the peripheral blood samples from carrier
pregnant women.
N. Fuchi, K. Miura, T. Tsukiyama,
D. Sasaki, N. Inokuchi, K. Yanagihara, S. Kamihira,
H. Moriuchi, K. Yoshiura, H. Masuzaki.
2880
T Characterization of placenta-specific
microRNAs in fetal growth restriction pregnancy.
A. Higashijima, K. Miura, H. Mishima, A. Kinoshita, O. Jo,
S. Abe, Y. Hasegawa, S. Miura, K. Yamasaki, A. Yoshida,
K. Yoshiura, H. Masuzaki.
2881
W Heritability of cardiovascular diseases in a
preeclampsia family cohort.
L. C. V. Thomsen, P. E.
Melton, K. Tollaksen, I. Lyslo, P. Solberg, L. T. Roten,
A. S. Gundersen, M. L. Odland, K. M. Strand, O. K.
Nygård, C. Sun, A.-C. Iversen, R. Austgulen, E. K.
Moses, L. Bjørge.
2856
T Cordocentesis: An alternative prenatal
procedure for women who missed amniocentesis in
developing regions of China.
Q. Cao, J. Ge, Y.-Y. Peng,
E. C. Jenkins, W. T. Brown, N. Zhong.
2857
W Single nucleotide polymorphism-based non-
invasive prenatal testing detects triploidy: Two case
studies.
Z. Demko, M. P. Hall, M. Hill, B. Zimmermann, S.
Sigurjonsson, M. Rabinowitz.
2858
T Prenatal diagnosis of 23 cases of microduplication
22
q11.2.
C. Dupont, F. Grati, K. W. Choy, S. Jaillard, J.
Toutain, M. L. Maurin, J. A. Martinez-Conejero, C. Beneteau,
D. Molina-Gomes, N. Horelli-Kuitunen, A. Aboura, C.
Baumann, E. Blondeel, B. Bessieres-Grattagliano, A. C.
Tabet, G. Simoni, B. Benzacken, F. Vialard.
2859
W Validation of epigenetic marker for noninvasive
prenatal diagnosis of fetal trisomy 18.
D. E. Lee, S. Y.
Kim, J. H. Lim, H. J. Kim, S.. Park, H. M. Ryu.
2860
T Highly accurate non-invasive detection of
fetal aneuploidy for chromosomes 13, 18, 21, X and
Y.
B. Levy, S. McAdoo, B. Zimmermann, M. Banjevic, B.
Pettersen, M. Hall, Z. Demko, M. Hill, M. Rabinowitz.
2861
W Disease-specific characteristics of fetal
epigenetic markers for non-invasive prenatal diagnosis
of trisomy 21.
J. Lim, D. Lee, S. Park, D. Kim, H. Kim, H.
Ahn, S. Lee, K. Choi, M. Kim, H. Ryu.
2862
T The concerns of health professionals and
pregnant women involving the non-invasive prenatal
diagnosis of trisomy 21 in Quebec and in France.
A. K.
Maglo, R. Drouin, J. M. Moutquin, C. Bouffard.
2863
W A single nucleotide polymorphism-based
approach to non-invasive prenatal testing identifies
lingering cell-free fetal DNA in pregnancies with
vanishing twins.
S. McAdoo, M. Savage, M. P. Hall, B.
Zimmermann, S. Sigurjonsson, Z. Demko, M. Rabinowitz.
2864
T A key role for amniotic fluid citrulline analysis
in the prenatal diagnosis of citrullinemia type I.
M. J.
Miller, V. R. Sutton, Q. Sun, S. H. Elsea.
2865
W Experience using a rapid assay for aneuploidy
and microdeletion detection in over 2900 prenatal
specimens.
S. Sulpizio, S. A. Morton, A. M. Bandholz,
L. D. McDaniel, R. A. Schultz, B. S. Torchia, J. B. Ravnan,
J. W. Ellison, P. Mowery-Rushton, J. A. Rosenfeld.
2866
T Methods for fetal fraction quantification in
circulating cell-free DNA sequencing libraries.
J. Tynan,
G. Hogg, J. Fox, P. Iyer, M. Ehrich.
2867
W Prenatal MLPA screening and aCGH analysis
detected cytogenomic abnormalities in four cases
with fetal ultrasound anomalies.
J. Xie, Z. Xu, Q. Geng,
F. Xu, P. Li.
2868
T Chinese Alliance of Translational Medicine for
Maternal and Children’s Health: A unique resource for
longitudinal cohort study of pregnancies.
J. Pan, Q.-X.
Shi, Y. Gu, X.-C. Lou, M.-F. Hua, N. Zhong.