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CNKI学位论文(42)
知网期刊论文(15)
在“
Elsevier电子期刊
”中,
命中:
31
条,耗时:小于0.01 秒
在所有数据库中总计命中:
57
条
1.
Monosomy
9pter and trisomy 9q34.
11q
ter in two sisters due to a maternal pericentric inversion
作者:
Farmaditya E.P. Mundhofir
a
;
b
;
Dominique Smeets
a
;
Willy Nillesen
a
;
Tri Indah Winarni
b
;
Helger G. Yntema
a
;
Nicole de Leeuw
a
;
Ben C.J. Hamel
a
;
Sultana M.H. Faradz
b
;
Bregje W.M. van Bon
a
;
B.vanBon@antrg.umcn.nl
关键词:
CEBIOR
;
Center for Biomedical Research
;
CNAG
;
Copy Number Analyzer for Affymetrix Genechip mapping
;
DECIPHER
;
Database of chromosomal imbalance and phenotype in humans using Ensembl Resources
;
DGHE
;
Directorate of Higher Education
;
DGV
;
Database of Genomi
刊名:Gene
出版年:2012
2.
Prenatal Diagnosis of Partial Trisomy 3p (3p21→pter) and Partial
Monosomy
11q
(
11q
23→qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System
作者:
Chih-Ping Chen
;
Tzu-Hao Wang
;
Chyi-Chyang Lin
;
Fuu-Jen Tsai
;
Lie-Jiau Hsieh
;
Wayseen Wang
关键词:
duplex renal system
;
holoprosencephaly
;
orofacial clefts
;
partial
monosomy
11q
;
partial trisomy 3p
;
pyelectasis
刊名:Journal of the Formosan Medical Association
出版年:2008
3.
Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome
作者:
Kalliopi N. Manola
a
;
pmanola@ipta.demokritos.gr
;
Fotios Panitsas
b
;
Sophia Polychronopoulou
c
;
Aggeliki Daraki
a
;
Maria Karakosta
a
;
Cryssa Stavropoulou
a
;
Georgia Avgerinou
c
;
Emmanuel Hatzipantelis
d
;
Gabriel Pantelias
a
;
Constantina Sambani
a
;
Maria Pagoni
b
关键词:
Cytogenetics
;
childhood and adolescent AML
;
outcome
;
monosomal karyotypes
刊名:Cancer Genetics
出版年:2013
4.
An emerging phenotype of proximal
11q
deletions
作者:
Daniela Melis
;
Rita Genesio
;
Mariarosaria Cozzolino
;
Ennio Del Giudice
;
Angela Mormile
;
Floriana Imperati
;
Valentina Ronga
;
Roberto Della Casa
;
Lucio Nitsch
;
Generoso Andria
关键词:
11q
monosomy
;
Interstitial deletion
刊名:European Journal of Medical Genetics
出版年:2010
5.
Prenatal diagnosis of mosaicism for
11q
terminal deletion
作者:
M. Valduga
;
V. Latger Cannard
;
C. Philippe
;
S. Romana
;
A. Miton
;
P. Droulle
;
B. Foliguet
;
T. Lecompte
;
P. Jonveaux
关键词:
11q
ter deletion mosaicism
;
Prenatal diagnosis
;
Jacobsen syndrome
;
Paris–
;
Trousseau syndrome
刊名:European Journal of Medical Genetics
出版年:2007
6.
Amplification of the RARA gene in acute myeloid leukemia: significant finding or coincidental observation?
作者:
Anna D. Asleson
;
Vickie Morgan
;
Stephen Smith
;
Gopalrao V.N. Velagaleti
刊名:Cancer Genetics and Cytogenetics
出版年:2010
7.
Specific chromosomal aberrations in de novo acute myeloid leukemia: A comparative analysis of results with a report of three novel chromosomal rearrangements t(7;14)(q35;q13), t(8;18)(p11.2;q12), t(13
作者:
Firoz Ahmad
;
Rupa Dalvi
;
Bibhu Ranjan Das
;
Swarna M
;
ava
关键词:
Acute myeloid leukemia
;
Chromosomal aberrations
;
Novel translocations
;
India
;
Clinical and biological features
;
Cytogenetics
刊名:Cancer Detection and Prevention
出版年:2008
8.
Frequency, hematopathology, and detection of a new isodicentric variant of deletion 20q
作者:
Stephanie A. Smoley
;
Stephanie R. Fink
;
Sarah F. Paternoster
;
Kimberly J. Stockero
;
Lai P. Nguyen
;
Phuong L. Nguyen
;
Curtis A. Hanson
;
Gordon W. Dewald
刊名:Cancer Genetics and Cytogenetics
出版年:2007
9.
Childhood myeloid leukaemias
作者:
Georgina W. Hall
关键词:
AML
;
11q
23
;
infant leukaemia
;
childhood MDS
;
monosomy
7
;
JMML
刊名:Best Practice & Research Clinical Haematology
出版年:2001
10.
Chromosome 11
monosomy
in conjunction with a mutated
SDHD
initiation codon in nonfamilial paraganglioma cases
作者:
Riemann
;
Kathrin
;
Sotlar
;
Karl
;
Kupka
;
Susan
;
Braun
;
Simone
;
Zenner
;
Hans-Peter
;
Preyer
;
Serena
;
et. al.
刊名:Cancer Genetics and Cytogenetics
出版年:2004
1
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