| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum
|
Lall, Meena
|
|
2011
|
4 |
1 |
|
article
|
| 2 |
An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype
|
Garcia, Daniela RN
|
|
2011
|
4 |
1 |
|
article
|
| 3 |
A rare case of t(11;22) in a mantle cell lymphoma like B-cell neoplasia resulting in a fusion of IGL and CCND1: case report
|
Rocha, Cristiano Krings
|
|
2011
|
4 |
1 |
|
article
|
| 4 |
Assessment of ERBB2 and EGFR gene amplification and protein expression in gastric carcinoma by immunohistochemistry and fluorescence in situ hybridization
|
YK, Wang
|
|
2011
|
4 |
1 |
|
article
|
| 5 |
Biclonal myelodysplastic syndrome involving six chromosomes and monoallelic loss of RB1 - A rare case
|
Al-Achkar, Walid
|
|
2011
|
4 |
1 |
|
article
|
| 6 |
Centrosomal and mitotic abnormalities in cell lines derived from papillary thyroid cancer harboring specific gene alterations
|
Maric, Irena
|
|
2011
|
4 |
1 |
|
article
|
| 7 |
Chromosomal mapping of rDNAs and H3 histone sequences in the grasshopper rhammatocerus brasiliensis (acrididae, gomphocerinae): extensive chromosomal dispersion and co-localization of 5S rDNA/H3 histone clusters in the A complement and B chromosome
|
Oliveira, Nathalia L
|
|
2011
|
4 |
1 |
|
article
|
| 8 |
Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects
|
Al-Zahrani, Jawaher
|
|
2011
|
4 |
1 |
|
article
|
| 9 |
Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases
|
Park, Sang-Jin
|
|
2011
|
4 |
1 |
|
article
|
| 10 |
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
|
Manolakos, Emmanouil
|
|
2011
|
4 |
1 |
|
article
|
| 11 |
Combined 22q11.1-q11.21 deletion with 15q11.2-q13.3 duplication identified by array-CGH in a 6 years old boy
|
Manolakos, Emmanouil
|
|
2011
|
4 |
1 |
|
article
|
| 12 |
Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells
|
Valli, Roberto
|
|
2011
|
4 |
1 |
|
article
|
| 13 |
Context-based FISH localization of genomic rearrangements within chromosome 15q11.2q13 duplicons
|
Khan, Wahab A
|
|
2011
|
4 |
1 |
|
article
|
| 14 |
De novo 7p partial trisomy characterized by subtelomeric FISH and whole-genome array in a girl with mental retardation
|
S, Aswini
|
|
2011
|
4 |
1 |
|
article
|
| 15 |
Diversity of sex chromosome abnormalities in a cohort of 95 Indonesian patients with monosomy X
|
Marzuki, Nanis S
|
|
2011
|
4 |
1 |
|
article
|
| 16 |
DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation
|
Kato, Takema
|
|
2011
|
4 |
1 |
|
article
|
| 17 |
Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis
|
Schultz, Roger A
|
|
2011
|
4 |
1 |
|
article
|
| 18 |
Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis
|
Kolquist, Kathryn A
|
|
2011
|
4 |
1 |
|
article
|
| 19 |
Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia
|
Bajaj, Renu
|
|
2011
|
4 |
1 |
|
article
|
| 20 |
Frequency of the 7q11.23 inversion polymorphism in transmitting parents of children with Williams syndrome and in the general population does not differ between North America and Europe
|
Morris, Colleen A
|
|
2011
|
4 |
1 |
|
article
|
| 21 |
Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10
|
Weimer, Jörg
|
|
2011
|
4 |
1 |
|
article
|
| 22 |
Molecular cytogenetic analysis and clinical manifestations of a case with de novo mosaic ring chromosome 7
|
Tsai, Li-Ping
|
|
2011
|
4 |
1 |
|
article
|
| 23 |
Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis
|
Van Opstal, Diane
|
|
2011
|
4 |
1 |
|
article
|
| 24 |
New cytogenetically visible copy number variant in region 8q21.2
|
Manvelyan, Marina
|
|
2011
|
4 |
1 |
|
article
|
| 25 |
On the origin of crossover interference: A chromosome oscillatory movement (COM) model
|
Hultén, Maj A
|
|
2011
|
4 |
1 |
|
article
|
| 26 |
Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect
|
Srebniak, Malgorzata I
|
|
2011
|
4 |
1 |
|
article
|
| 27 |
Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report
|
Krgovic, Danijela
|
|
2011
|
4 |
1 |
|
article
|
| 28 |
The genome diversity and karyotype evolution of mammals
|
Graphodatsky, Alexander S
|
|
2011
|
4 |
1 |
|
article
|
Journal description