Works matching IS 17558166 AND DT 2011 AND VI 4 AND IP 1

Results: 28

Prenatally diagnosed submicroscopic familial aberrations at 18p11.32 without phenotypic effect.

Published in:: 2011
Publication type:: Case Study

Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 28, doi. 10.1186/1755-8166-4-28
Publication type:: Article

Evaluation of chronic lymphocytic leukemia by oligonucleotide-based microarray analysis uncovers novel aberrations not detected by FISH or cytogenetic analysis.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 25, doi. 10.1186/1755-8166-4-25
Publication type:: Article

Centrosomal and mitotic abnormalities in cell lines derived from papillary thyroid cancer harboring specific gene alterations.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 26, doi. 10.1186/1755-8166-4-26
Publication type:: Article

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.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 24, doi. 10.1186/1755-8166-4-24
Publication type:: Article

Diversity of sex chromosome abnormalities in a cohort of 95 Indonesian patients with monosomy X.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 23, doi. 10.1186/1755-8166-4-23
Publication type:: Article

The genome diversity and karyotype evolution of mammals.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 22, doi. 10.1186/1755-8166-4-22
Publication type:: Article

De novo 7p partial trisomy characterized by subtelomeric FISH and whole-genome array in a girl with mental retardation.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 21, doi. 10.1186/1755-8166-4-21
Publication type:: Article

An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype.

Published in:: 2011
Publication type:: Case Study

A 54 Mb 11qter duplication and 0.9 Mb 1q44 deletion in a child with laryngomalacia and agenesis of corpus callosum.

Published in:: 2011
Publication type:: Case Study

DNA secondary structure is influenced by genetic variation and alters susceptibility to de novo translocation.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 18, doi. 10.1186/1755-8166-4-18
Publication type:: Article

Submicroscopic interstitial deletion of chromosome 11q22.3 in a girl with mild mental retardation and facial dysmorphism: Case report.

Published in:: 2011
Publication type:: Case Study

Biclonal myelodysplastic syndrome involving six chromosomes and monoallelic loss of RB1 - A rare case.

Published in:: 2011
Publication type:: Case Study

Context-based FISH localization of genomic rearrangements within chromosome 15q11.2q13 duplicons.

Published in:: Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 15, doi. 10.1186/1755-8166-4-15
Publication type:: Article

Assessment of ERBB2 and EGFR gene amplification and protein expression in gastric carcinoma by immunohistochemistry and fluorescence in situ hybridization.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 14, doi. 10.1186/1755-8166-4-14

By:

Wang, Y. K.;
Gao., C. F.;
Yun, T.;
Chen, Z.;
Zhang, X. W.;
Lv, X. X.;
Meng, N. L.;
Zhao, W. Z.

Publication type:

Article

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 12, doi. 10.1186/1755-8166-4-12

By:

Park, Sang-Jin;
Eun Hye Jung;
Ryu, Ran-Suk;
Hyun Woong Kang;
Jung-Min Ko;
Kim, Hyon J.;
Chong Kun Cheon;
Sang-Hyun Hwang;
Ho-Young Kang

Publication type:

Article

Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 13, doi. 10.1186/1755-8166-4-13

By:

Valli, Roberto;
Marletta, Cristina;
Pressato, Barbara;
Montalbano, Giuseppe;
Curto, Francesco Lo;
Pasquali, Francesco;
Maserati, Emanuela

Publication type:

Article

On the origin of crossover interference: A chromosome oscillatory movement (COM) model.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 10, doi. 10.1186/1755-8166-4-10

By:

Hultén, Maj A.

Publication type:

Article

Combined 22q11.1-q11.21 deletion with 15q11.2- q13.3 duplication identified by array-CGH in a 6 years old boy.

Published in:

2011

By:

Manolakos, Emmanouil;
Sarri, Catherine;
Vetro, Annalisa;
Kefalas, Konstantinos;
Leze, Eleni;
Sofocleus, Christalena;
Kitsos, George;
Merou, Konstantina;
Kokotas, Haris;
Papadopoulou, Anna;
Attilakos, Achilleas;
Petersen, Michael B.;
Kitsiou-Tzeli, Sofia

Publication type:

Correction Notice

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.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 9, doi. 10.1186/1755-8166-4-9

By:

Al-Zahrani, Jawaher;
Al-Dosari, Naji;
AbuDheim, Nada;
Alshidi, Tarfa A.;
Colak, Dilek;
Al-Habit, Ola;
Al-Odaib, Ali;
Sakati, Nadia;
Meyer, Brian;
Ozand, Pinar T.;
Kaya, Namik

Publication type:

Article

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.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 8, doi. 10.1186/1755-8166-4-8

By:

Rocha, Cristiano Krings;
Praulich, Inka;
Gehrke, Iris;
Hallek, Michael;
Kreuzer, Karl-Anton

Publication type:

Article

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.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 7, doi. 10.1186/1755-8166-4-7

By:

Morris, Colleen A.;
Mervis, Carolyn B.;
Osborne, Lucy R.

Publication type:

Article

Combined 22q11.1-q11.21 deletion with 15q11.2- q13.3 duplication identified by array-CGH in a 6 years old boy.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 6, doi. 10.1186/1755-8166-4-6

By:

Manolakos, Emmanouil;
Sarri, Catherine;
Vetro, Annalisa;
Kefalas, Konstantinos;
Leze, Eleni;
Sofocleus, Christalena;
Kitsos, George;
Merou, Konstantina;
Kokotas, Haris;
Papadopoulou, Anna;
Attilakos, Achilleas;
Petersen, Michael B.;
Kitsiou-Tzeli, Sofia

Publication type:

Article

Molecular cytogenetic analysis and clinical manifestations of a case with de novo mosaic ring chromosome 7.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 5, doi. 10.1186/1755-8166-4-5

By:

Li-Ping Tsai;
Kuei-Fang Lee;
Jye-Siung Fang;
Liu, Ingrid Y.

Publication type:

Article

Evaluation of chronic lymphocytic leukemia by BAC-based microarray analysis.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 4, doi. 10.1186/1755-8166-4-4

By:

Schultz, Roger A.;
Delioukina, Maria;
Gaal, Karl;
Bedell, Victoria;
Smith, David D.;
Forman, Stephen J.;
McDaniel, Lisa D.;
Ballif, Blake C.;
Shaffer, Lisa G.;
Slovak, Marilyn L.

Publication type:

Article

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 1, doi. 10.1186/1755-8166-4-3

By:

Bajaj, Renu;
Fang Xu;
Bixia Xiang;
Wilcox, Katherine;
DiAdamo, Autumn J.;
Kumar, Rachana;
Pietraszkiewicz, Alexandra;
Halene, Stephanie;
Peining Li

Publication type:

Article

Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 1, doi. 10.1186/1755-8166-4-2

By:

Van Opstal, Diane;
Boter, Marjan;
Noomen, Petra;
Srebniak, Malgorzata;
Hamers, Guus;
Galjaard, Robert-Jan H.

Publication type:

Article

New cytogenetically visible copy number variant in region 8q21.2.

Published in:

Molecular Cytogenetics (17558166), 2011, v. 4, n. 1, p. 1, doi. 10.1186/1755-8166-4-1

By:

Manvelyan, Marina;
Cremer, Friedrich W.;
Lancé, Jeannette;
Kläs, Rüdiger;
Kelbova, Christina;
Ramel, Christian;
Reichenbach, Herbert;
Schmidt, Catharina;
Ewers, Elisabeth;
Kreskowski, Katharina;
Ziegler, Monika;
Kosyakova, Nadezda;
Liehr, Thomas

Publication type:

Article