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Perinatal findings and molecular cytogenetic analysis ofde novo partial trisomy 16q (16q22.1?qter) and partial monosomy 20q (20q13.3?qter)
Prenatal Diagnosis
◽
10.1002/pd.1083
◽
2005
◽
Vol 25
(2)
◽
pp. 112-118
◽
Cited By ~ 11
Author(s):
Chih-Ping Chen
◽
Shuan-Pei Lin
◽
Chyi-Chyang Lin
◽
Yueh-Chun Li
◽
Schu-Rern Chern
◽
...
Keyword(s):
Cytogenetic Analysis
◽
Partial Trisomy
◽
Partial Monosomy
◽
Molecular Cytogenetic
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Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3→qter) and partial trisomy 18q (18q23→qter) in a fetus associated with cystic hygroma and ambiguous genitalia
Prenatal Diagnosis
◽
10.1002/pd.1179
◽
2005
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Vol 25
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◽
pp. 492-496
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Partial Trisomy
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Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly
Taiwanese Journal of Obstetrics and Gynecology
◽
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◽
2010
◽
Vol 49
(3)
◽
pp. 320-326
◽
Cited By ~ 18
Author(s):
Chih-Ping Chen
◽
Ming Chen
◽
Yi-Ning Su
◽
Fuu-Jen Tsai
◽
Schu-Rern Chern
◽
...
Keyword(s):
Prenatal Diagnosis
◽
De Novo
◽
Partial Trisomy
◽
Partial Monosomy
◽
Molecular Cytogenetic
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Skull Development
◽
Dandy Walker Malformation
◽
Cytogenetic Characterization
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Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature
Birth Defects Research Part A Clinical and Molecular Teratology
◽
10.1002/bdra.23213
◽
2014
◽
Vol 100
(4)
◽
pp. 284-293
◽
Cited By ~ 1
Author(s):
Stavros Sifakis
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Makarios Eleftheriades
◽
Dimitra Kappou
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Roberta Murru
◽
Anastasia Konstantinidou
◽
...
Keyword(s):
Prenatal Diagnosis
◽
Comparative Genomic Hybridization
◽
Cytogenetic Analysis
◽
Partial Trisomy
◽
Comparative Genomic
◽
Review Of The Literature
◽
Genomic Hybridization
◽
Comparative Genomic Hybridization Array
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Molecular Cytogenetic
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Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter)
Taiwanese Journal of Obstetrics and Gynecology
◽
10.1016/j.tjog.2016.02.015
◽
2016
◽
Vol 55
(2)
◽
pp. 288-292
◽
Cited By ~ 1
Author(s):
Chih-Ping Chen
◽
Fung-Yu Hung
◽
Schu-Rern Chern
◽
Peih-Shan Wu
◽
Yen-Ni Chen
◽
...
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Prenatal Diagnosis
◽
De Novo
◽
Partial Trisomy
◽
Partial Monosomy
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Molecular Cytogenetic
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Cytogenetic Characterization
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Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold
Gene
◽
10.1016/j.gene.2012.12.051
◽
2013
◽
Vol 516
(1)
◽
pp. 138-142
◽
Cited By ~ 6
Author(s):
Chih-Ping Chen
◽
Yi-Yung Chen
◽
Schu-Rern Chern
◽
Peih-Shan Wu
◽
Jun-Wei Su
◽
...
Keyword(s):
Prenatal Diagnosis
◽
De Novo
◽
Coarctation Of The Aorta
◽
Partial Trisomy
◽
Partial Monosomy
◽
Molecular Cytogenetic
◽
Cytogenetic Characterization
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Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35?qter: Molecular cytogenetic analysis and clinical phenotype in two generations
American Journal of Medical Genetics
◽
10.1002/1096-8628(20000828)93:5<349::aid-ajmg2>3.0.co;2-s
◽
2000
◽
Vol 93
(5)
◽
pp. 349-354
◽
Cited By ~ 18
Author(s):
Frank Speleman
◽
Brenda Callens
◽
Karel Logghe
◽
Nadine Van Roy
◽
Sharon W. Horsley
◽
...
Keyword(s):
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◽
Clinical Phenotype
◽
Partial Trisomy
◽
Molecular Cytogenetic
◽
Familial Translocation
◽
Two Generations
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Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q
American Journal of Medical Genetics Part A
◽
10.1002/ajmg.a.31329
◽
2006
◽
Vol 140A
(14)
◽
pp. 1594-1600
◽
Cited By ~ 30
Author(s):
Chih-Ping Chen
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Shuan-Pei Lin
◽
Chyi-Chyang Lin
◽
Yann-Jang Chen
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Schu-Rern Chern
◽
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Cytogenetic Analysis
◽
De Novo
◽
Partial Trisomy
◽
Review Of The Literature
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Molecular Cytogenetic
◽
Partial Trisomy 5Q
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Partial Trisomy 2p and Partial Monosomy 2q Arising from a Paternal Intrachromosomal 2q-into-2p Between-Arm Insertion and Paracentric Inversion: Molecular Cytogenetic Characterization of a Four-Break Rearrangement
Cytogenetic and Genome Research
◽
10.1159/000350868
◽
2013
◽
Vol 140
(1)
◽
pp. 12-20
Author(s):
E. Manolakos
◽
A. Vetro
◽
E. Papadopoulou
◽
K. Kefalas
◽
M. Lagou
◽
...
Keyword(s):
Partial Trisomy
◽
Paracentric Inversion
◽
Partial Monosomy
◽
Molecular Cytogenetic
◽
Cytogenetic Characterization
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Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)
Prenatal Diagnosis
◽
10.1002/pd.1399
◽
2006
◽
Vol 26
(4)
◽
pp. 313-320
◽
Cited By ~ 8
Author(s):
Chih-Ping Chen
◽
Schu-Rern Chern
◽
Chyi-Chyang Lin
◽
Tzu-Hao Wang
◽
Yueh-Chun Li
◽
...
Keyword(s):
Partial Trisomy
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Partial Monosomy
◽
Molecular Cytogenetic
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Cytogenetic Analyses
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Molecular cytogenetic analysis of feline leukemia virus insertions in cat lymphoid tumor cells
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◽
10.1016/j.jviromet.2009.10.021
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2010
◽
Vol 163
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◽
pp. 344-352
◽
Cited By ~ 2
Author(s):
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◽
Hitoshi Satoh
◽
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◽
Cytogenetic Analysis
◽
Leukemia Virus
◽
Feline Leukemia Virus
◽
Lymphoid Tumor
◽
Molecular Cytogenetic
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