Page 246 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
235
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
2990
T Identification of messenger RNA of fetoplacental
source in maternal plasma of women with normal
pregnancies and pregnancies with intrauterin growth
restriction.
P. Ayala Ramírez, R. García Robles, J. D.
Rojas, M. Bermúdez, J. Bernal Villegas.
2991
T Instant familial haplotyping in conjunction with
embryo analysis in preimplantation genetic diagnosis
using DNA microarrays.
G. Altarescu, D. A. Zeevi, S.
Zeligson, S. Perlberg, T. Eldar-Geva, E. J. Margalioth, E.
Levy Lahad, P. Renbaum.
2992
T Role of cytokines in recurrent miscarriages.
F.
Parveen, S. Agrawal.
2993
T Developmental neuropsychological assessment
of 4-5-year-old children born after preimplantation
genetic diagnosis: A pilot study.
G. Sacks, J. Guedalia,
T. Eldar-Geva, T. Gilboa, E. J. Margalioth, E. Levy-Lahad,
G. Altarescu.
2994
T Terminological clarification in PGD: Could it
reframe the debate?
S. Côté, P. Hamet.
2995
T A novel, generic, preimplantation genetic
diagnosis protocol applied to cystic fibrosis involving
mutation detection through high resolution melting
analysis and simultaneous haplotype analysis through
QF-PCR.
A. Destouni, M. Poulou, G. Kakourou, C. Vrettou,
J. Traeger-Synodinos, I. Fylaktou, E. Kanavakis, M. Tzetis.
2996
T PGD and heteroplasmic mitochondrial DNA
point mutations: A systematic review estimating the
chance of healthy offspring.
D. M. E. I. Hellebrekers, R.
Wolfe, A. T. M. Hendrickx, I. F. M. de Coo, C. E. de Die, J.
P. M. Geraedts, P. F. Chinnery, H. J. M. Smeets.
2997
T Successful pre-implantation genetic diagnosis
in isolated sulfite oxidase deficiency: A happy end to
the saga of a devastating neurogenetic disorder.
A.
Kondkar, K. Abu-Amero, M. Salih, T. Bosley.
2998
T Outcomes of 687 in vitro fertilization cycles and
5871
embryos evaluated using 23-chromosome single
nucleotide polymorphism microarray preimplantation
genetic screening for recurrent pregnancy loss.
K. J.
Tobler, P. R. Brezina, A. T. Benner, L. Du, B. Boyd, W. G.
Kearns.
2999
T Cleavage-stage blastomere biopsy significantly
impairs human embryonic reproductive potential
while blastocyst-stage trophectoderm biopsy does
not: A paired randomized controlled trial utilizing SNP
microarray-based DNA fingerprinting.
N. R. Treff, K. M.
Ferry, T. Zhao, J. Su, E. J. Forman, R. T. Scott, Jr.
3000
T Comparison of two whole genome amplification
methods for preimplantation genetic diagnosis with
HLA typing on beta-thalassaemia.
Q. Wang, J. F. C.
Chow, W. S. B. Yeung, E. H. Y. Ng, P. C. Ho.
3001
T Preimplantation genetic diagnosis for a carrier
of complex chromosome rearrangement resulting in a
healthy offspring.
K. Writzl, A. Veble, B. Peterlin.
2977
T Functional consequences of miscarriage copy
number variations.
J. Wen, C. W. Hanna, S. Martell, P. C.
K. Leung, W. P. Robinson, M. Stephenson, E. Rajcan-
Separovic.
2978
T The fetal fraction of cell-free DNA in maternal
plasma is not affected by a priori risk of fetal trisomy.
T. Musci, H. Brar, E. Wang, B. Brar, A. Y. Batey, A.
Oliphant, M. E. Norton.
2979
T Role of E2F1 in testicular descent and fertility.
C.
Jorgez, J. Addai, J. Newberg, V. Vangapandu, A. Sahin, J.
Rosenfeld, L. Lipshultz, D. Lamb.
2980
T Study of four SNPs in
SLC6A14, INSR, TAS2R38
and
OR2W3
genes for association with Iranian
idiopathic infertile men.
E. Siasi, A. Aleyasin.
2981
T
NLRP7
subcellular localization in human oocytes
and early cleavage stages.
E. Akoury, L. Zhang, M.
Seoud, A. Ao, R. Slim.
2982
T Human spermatogenic failure purges
deleterious mutation load from the autosomes and
both sex chromosomes, including the gene
DMRT1
.
D. F. Conrad, A. Lopes, K. I. Aston, F. Carvalho, J.
Goncalves, R. Mathiesen, N. Huang, A. Ramu, J. Downie,
S. Fernandes, A. Amorim, A. Barros, M. Hurles, S.
Moskovtsev, C. Ober, J. Schiffman, P. N. Schlegel, M. De
Sousa, D. T. Carrell.
2983
T A homozygous deletion of
DPY19L2
gene is a
cause of globozoospermia in men from the Republic
of Macedonia.
D. Plaseska-Karanfilska, P. Noveski, S.
Madjunkova, I. Maleva, V. Sotiroska, Z. Petanovski.
2984
T Decreased puberty and fertility development
in NELF KO mice due to impaired GnRH neuron
migration.
S. Quaynor, L. Chorich, R. Cameron, L.
Layman.
2985
T Deficiency of PRSS37, a putative trypsin-like
serine protease, causes male infertility from mouse to
human.
Z. G. Wang, C. L. Shen, J. B. Liu, J. S. Feng, Y.
Kuang, H. X. Zhang, W. T. Wu, J. Chi, L. Y. Tang, J. Fei.
2986
T Changes in placental DNA methylation may be
associated with karyotypically normal miscarriage.
C.
W. Hanna, D. E. McFadden, W. P. Robinson.
2987
T Co-culture of mouse embryonic stem cells with
Sertoli cells promote in vitro generation of germ cells.
M. Miryounesi, K. Nayernia, M. Dianatpour, S. Savad, M.
H. Modarressi.
2988
T Androgen receptor CAG repeat length may
influence the risk of polycystic ovarian syndrome.
J. C.
Silas, R. Singh, S. Nirmala Sadasivam, M. N. Sadasivam,
L. Singh, K. Thangaraj.
2989
T An analysis of the initial experience offering cell-
free fetal DNA testing to pregnant women.
J. Taylor, A.
Ables, L. Hudgins.