Page 163 - ASHG 2012 Annual Meeting Program Guide

152
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
1036
T C-MYC and IGH amplification in patients with
intermediate high grade B-cell lymphomas.
A. Zaslav,
M. Bellone, F. Lan, T. Mercado, H. Lee, Y. Hu.
1037
F Two deletions in the
APC
gene (an inherited
deletion in exon 1 and a de novo deletion in exon
12)
and a de novo
MUTYH
deletion causing familial
adenomatous polyposis.
G. A. Molfetta, O. C. Vincenzi,
J. Huber, A. A. Marques, W. A. Silva, Jr.
1038
W Mutation screening in adenomatous polyposis
coli gene in patients clinically diagnosed as familial
adenomatous polyposis.
O. C. Vincenzi, G. A. Molfetta,
J. Huber, C. Ayres, W. A. Silva, Jr.
1039
T High-precision CNV analysis of FFPE samples
with the nCounter Analysis System.
G. Geiss.
1040
F Germline copy number variation in high-risk
African American families with prostate cancer.
E.
Ledet, X. Hu, O. Sartor, W. Rayford, M. Li, D. Mandal.
1041
W
hapLOH
:
Powerful haplotype-based profiling of
allelic imbalance in impure tumor samples.
P. Scheet,
R. Xia, S. Vattathil.
1042
T Protein tyrosine phosphatase receptor type J is
implicated in lymphomagenesis of follicular and diffuse
large B-cell lymphomas.
C. A. Aya-Bonilla, M. R. Green,
E. Camilleri, M. Benton, C. Keane, P. Marlton, R. Lea, M. K.
Gandhi, L. R. Griffiths.
1043
F Computational techniques to detect BFB in
tumor genomes.
S. Zakov, M. Kinsella, V. Bafna.
1044
W Evaluation of cytogenetic and gene
polymorphic variants in workers occupationally
exposed to silica-stone quarry industry.
R.
Chandirasekar, K. Sasikala, B. Lakshman Kumar, R.
Raichel Jacob, H. Kavitha.
1045
T Differential expression of
AURKA
and
AURKB
genes in bone marrow stromal mesenchymal cells of
myelodisplastic syndrome: Correlation with G-banding
analysis and FISH.
F. M. Oliveira, A. R. Lucena-Araujo,
M. C. Favarin, E. M. Rego, R. P. Falcão, B. P. Simıes, D. T.
Covas, A. M. Fontes.
1046
F A new function for the VHL tumor suppressor
protein: Prevention of genome instability through
promotion of homologous recombinational DNA repair.
M. S. Meyn, J. L. Metcalf, P. S. Bradshaw, M. Komosa, S.
N. Greer, W. Y. Kim, M. Ohh.
1047
W A new role for the ATM protein: Homologous
recombination repair of DNA damage.
P. Bradshaw, M.
Komosa, M. S. Meyn.
1048
T A crosstalk between ATM and FA/BRCA proteins
is necessary to preserve DNA integrity during G2/M
phase.
L. C. Torres Maldonado, D. Sosa, M. Castañon, A.
Rodriguez, B. Molina, C. Lopez Camarillo, S. Frias.
1049
F A dynamic model of the FA/BRCA DNA repair
pathway.
A. Rodriguez, L. Torres, D. Sosa, E. Cortes, A.
Biloglav, E. Forestier, K. Paulsson, B. Johansson.
1024
T Loss of chromosomes is the primary event in
near-haploid and low hypodiploid acute lymphoblastic
leukemia.
S. Safavi, E. Forestier, I. Golovleva, G. Barbany,
K. H. Nord, A. V. Moorman, C. J. Harrison, B. Johansson,
K. Paulsson.
1025
F Detection of the t(8;14) chromosomal
rearrangements in paraffin embedded tissue sections
of Burkitt lymphoma patients with quantitative
polymerase chain reaction and fluorescence in situ
hybridization methods.
N. Selvi, M. Hekimgil, B. Tezcanli
Kaymaz, S. Aktas, N. Ozhan, C. Gunduz, B. Kosova, Y.
Dodurga, N. Topcuoglu.
1026
W Molecular changes in Lynch syndrome
associated and sporadic ovarian carcinomas.
A.
Tieva, S. Kaur, L. Renkonen-Sinisalo, H. J. Järvinen, J.-P.
Mecklin, R. Bützow, P. Peltomäki.
1027
T A comprehensive genetic and epigenetic
study of hepatocellular carcinoma with microarrays.
G. Zhang, C. Wu, D. Yu, J. Chang, W. Sun, M. Li, L. Liang,
Y. Li, D. Lin.
1028
F Congenital leukemia with insertion of
MLL
into
19
p13.3 and a deletion of half a megabase of 19p13.3:
Case report.
H. Al-Kateb, M. Evenson, S. Kulkarni.
1029
W Cytogenetic profiles of 370 cases with renal cell
carcinoma: UCLA experience.
P. H. Bui, P. N. Rao.
1030
T Identifying of cryptic genomic alterations by
high-resolution microarrays in LLA-B and LLA-T
Mexican patients.
C. Córdova-Fletes, B. Macias-García,
A. Lugo-Trampe, N. Mendez-Ramírez, R. De la Rosa-
Alvarado, H. Gutiérrez-Aguirre, D. Gómez-Almaguer, A.
Hidalgo, R. Salazar-Riojas, P. Ruíz-Flores, P. Villarreal-
Quiroga, O. González-Llano, A. Rojas-Martínez, H.
Decanini-Arcaute, R. Ortiz-López.
1031
F An unusual case of APL in a 14-year-old girl with
t(15;17)(q22;q21) and t(9;22)(q34;q11.2).
V. Jobanputra,
C. Freeman, S. Hussein, M. J. Macera, B. Levy, V. V. Murty,
M. L. Sulis, G. Bhagat.
1032
W Integration of cytogenetics and FISH studies
for accurate evaluation of chromosome abnormalities.
N. Qin, M. Hibbard.
1033
T Evaluation of
FGFR1
gene amplification status
and its association with clinicopathological features in
breast cancer.
R. M. Rodrigues-Peres, J. K. Heinrich, L.
O. Z. Sarian.
1034
F Large scale identification of chromosomal
abnormalities in familial breast and ovarian cancer.
H.
W. H. Yin, L. L. Wang, E. Tsui, Y. Elshimali, D. C. Chen.
1035
W Homozygous deletions of
CDKN2A
are present
in all dic(9;20)(p13.2;q11.2)-positive BCP ALLs and
may be important for leukemic transformation.
V. Zachariadis, J. Schoumans, G. Barbany, M. Heyman, E.
Forestier, B. Johansson, M. Nordenskjöld, A. Nordgren.