Page 156 - ASHG 2012 Annual Meeting Program Guide

POSTER SESSIONS
145
POSTER SESSIONS
W=Wednesday authors will present; T=Thursday authors will present; F=Friday authors will present
Kim, J. Kim, S. Yoon.
868
T Detection of donor cells with a clonal
abnormality 20 years after transplantation: Is this
evidence of donor cell leukemia?
G. Velagaleti, V.
Ortega, D. Means.
869
W Xp22.31 duplications: Indistinctly benign or
inconspicuously pathogenic?
E. D. Esplin, B. Li, V. Cox,
R. Clark, C. Curry, A. Slavotinek, L. Hudgins.
870
T Refining the critical region associated with
Jacobsen syndrome through the identification of a
small interstitial deletion at 11q23.4-q24.1 by CGH
array.
S. Raskin, H. Salomão, F. R. Faucz, A. Bonalumi, J.
Souza, P. Grossfeld, J. Rosenfeld, V. S. Sotomaior.
871
W Triploid-diploid mixoploidy presenting with
gastrointestinal complaints and growth failure.
F. I.
Bhamani, G. L. Elsner, M. B. Beg, R. R. Lebel.
872
T Trisomy 14 mosaicism in a girl: Clinical
cytogenetic and molecular analysis.
R. Cruz-Alcivar, E.
Lieberman, C. Salas, M. P. Navarrete Meneses, C. Cantú,
K. Buiting, C. Durán-McKinster, V. Del Castillo-Ruiz, P.
Pérez-Vera, Alcivar.
873
W Low Klinefelter mosaicism in a male with
azoospermia detected by FISH.
P. A. Delgado, B.
Crandall, N. Rao, P. Bui, C. A. Tirado.
874
T A balanced translocation t(2;16)(q35;q24.1)
associated with limb defects and craniofacial
dysmorphism through presumptive misregulation of
the
IHH
(
Indian hedgehog) gene.
A. C. S. Fonseca, S.
Antonini, A. Bonaldi, P. A. Otto, A. M. Vianna-Morgante.
875
W Detection of parental origin and meiotic error
type in abortions and born alive with aneuploidies.
S.
Frias, S. P. Mendoza-Constantino, S. Sánchez, L. Torres,
B. Molina, P. Grether, D. G. Mayén, R. Meléndez, E.
Yokoyama, C. Villarroel, E. Lieberman, V. del Castillo.
876
T Non-mosaic trisomy 9: A new case report.
T.
Greer, B. Powell, N. Hauser, J. Shen, L. Mahon, R. Owen,
T. Sahoo, A. Anguiano, F. Boyar.
877
W A unique phenotype of 2q24.3-2q32.1
duplication: Infantile-onset epilepsy without mesomelic
dysplasia.
B. Lim, J. Ko, J. Choi, M. Woo, J. Chae.
878
T Importance of chromosome breakage testing
in Fanconi’s anemia: Involvement of specific
chromosomes.
V. Mohan, G. Archana, T. Preethi.
879
W Collaborative multicenter cytogenetic study of
microdeletion syndromes: Brazilian Network.
M. Riegel,
N. Barcellos, R. Mergener, R. Gus, R. Giugliani, Brazilian
Network Members.
880
T Iidentification of chromosome aberration
in fragile X syndrome patients in Tamil Nadu
population South India using cytogenetic techniques.
A. Sundramoorthy.
Cytogenetics
855
W Evaluation of vitamin B12 effects on DNA
damage induced by paclitaxel.
O. Khabour, K. Alzoubi,
M. Khader.
856
T Evaluation of vitamin B12 effects on DNA damage
induced by pioglitazone.
K. Alzoubi, O. Khabour, N.
Hussain, S. Al-azzam, N. Mhaidat.
857
W Cytogenetic study of induced pluripotent
stem cells derived from senescent cells of elderly
persons.
F. Pellestor, L. Lapasset, F. Becker, J.
Puechberty, A. Schneider, S. Taviaux, P. Sarda, J. M.
Lemaitre, G. Lefort.
858
T Secondary aneuploidy in samples of balanced
chromosomal rearrangements: No increased rate
detected.
O. Reish, R. Amiran, A. Kanesky, S. Gerafi, M.
Mashevich.
859
W Telomere “loss” in people with Down syndrome
with and without mild cognitive impairment more than
doubles after T-lymphocytes have been frozen in liquid
nitrogen and short-term cultured with PHA.
E. Jenkins,
L. Ye, S. Krinsky-McHale, W. Zigman, N. Schupf, W.
Silverman.
860
T Study of aging consequences in human
mesenchymal stem cells during tandem passages.
H.
Pour-Jafari, B. Pourjafari, F. Talebzadeh, A.R. Zamani, M.
Hosseinipanah, H. Fazli.
861
W Telomere structure and function in Cornelia
de Lange syndrome preserved despite evidence
for premature aging.
A. D. Kline, H. Riethman, K.
Ravichandran, M. Kaur, A. Kimball, I. D. Krantz.
862
T Identifying genes associated with hearing loss
through chromosomal translocations.
B. B. Currall,
N. G. Robertson, A. M. Lindgren, M. E. Talkowski, C. C.
Morton.
863
W An unbalanced whole-arm translocation
der(1;13)(q10;q10) in Burkitt lymphoma.
Y. Seok, S. J.
Park, S. J. Kim, E. Y. Lee, J. R. Choi.
864
T Two sibs with trisomy 2q 34-qter.
Y. Wang, X. He,
Y. Zhou, C. Wang, X. Yang, L. Zhu, Y. Yang, H. Wu, X. Liu,
D. Shrestha, C. Lee, E. Carter, J. Martinez.
865
W Subtelomere sequences on human acrocentric
chromosome short arms.
S. Baaj, A. Clarke, P.
Thakkar, E. Chan, M. Khan, S. Chawla, J. Leya,
J. Doering.
866
T Multiple chromosomal losses and gain including
the deletion of 12p13 region defined by cytogenetic
microarray in a case of simultaneous T-cell
prolymphocytic leukemia and renal cell carcinoma.
J.
Kim, J. Moon, M. Nam, J. Kim, S. Yoon.
867
W A case of therapy-related acute myeloid
leukemia with t(19;21)(q13.4;q22).
M. Nam, J. Moon, J.