Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set
about
Comprehensive characterization of evolutionary conserved breakpoints in four New World Monkey karyotypes compared to Chlorocebus aethiops and Homo sapiensCentromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics.Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair.X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanationPartial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl.High-throughput sequencing of microdissected chromosomal regions.Novel Cryptic Rearrangements in Adult B-Cell Precursor Acute Lymphoblastic Leukemia Involving the MLL Gene.High rates of submicroscopic aberrations in karyotypically normal acute lymphoblastic leukemia.Complex translocation involving four chromosomes in a novel Philadelphia-positive chronic myeloid leukemia case.A rare chronic myeloid leukemia case with Philadelphia chromosome, BCR-ABL e13a3 transcript and complex translocation involving four different chromosomes.Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome.Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex.A new t(9;11;20;22)(q34;p11.2;q11.21;q11) in a Philadelphia-positive chronic myeloid leukemia case.A novel IGH@ gene rearrangement associated with CDKN2A/B deletion in young adult B-cell acute lymphoblastic leukemia.First molecular cytogenetic high resolution characterization of the NIH 3T3 cell line by murine multicolor bandingA de novo acute myeloid leukemia (AML-M4) case with a complex karyotype and yet unreported breakpoints.Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report.Human Ring Chromosomes - New Insights for their Clinical Significance.Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report.First detailed reconstruction of the karyotype of Trachypithecus cristatus (Mammalia: Cercopithecidae)The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2.Diagnostic applications of fluorescence in situ hybridization.Fluorescence in situ hybridization techniques in medical diagnostics.Multicolor FISH methods in current clinical diagnostics.Conventional and molecular cytogenetic characterization of Burkitt lymphoma with bone marrow involvement in Brazilian children and adolescents.X-autosome and X-Y Translocations in Female Carriers: X-chromosome Inactivation Easily Detectable by 5-ethynyl-2-deoxyuridine (EdU)A unique complex translocation involving six different chromosomes in a case of childhood acute lymphoblastic leukemia with the Philadelphia chromosome and adverse prognosis.A rare case of Philadelphia chromosome-positive chronic myelogenous leukemia with inversion in chromosome 9 and t(10;17).A Novel Cryptic Three-Way Translocation t(2;9;18)(p23.2;p21.3;q21.33) with Deletion of Tumor Suppressor Genes in 9p21.3 and 13q14 in a T-Cell Acute Lymphoblastic Leukemia.A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12).Evidence for correlation of fragile sites and chromosomal breakpoints in carriers of constitutional balanced chromosomal rearrangements.Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes.The hierarchically organized splitting of chromosomal bands for all human chromosomes.The prognostic role of hemochromatosis H63D allele in allogeneic hematopoietic stem cell transplantation.A family with an inverted tandem duplication 5q22.1q23.2.Exceptional Chromosomal Evolution and Cryptic Speciation of Blind Mole Rats Nannospalax leucodon (Spalacinae, Rodentia) from South-Eastern Europe.Characterization of a complex chromosomal rearrangement involving chromosomes 1, 3, and 4 in a slightly affected male with bad obstetrics history.Multicolor Karyotyping and Fluorescence In Situ Hybridization-Banding (MCB/mBAND).Five Novel Locations of Neocentromeres in Human: 18q22.1, Xq27.1~27.2, Acro p13, Acro p12, and Heterochromatin of Unknown Origin
P2860
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P2860
Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set
description
2008 nî lūn-bûn
@nan
2008 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Molecular definition of high-r ...... nchored FISH banding probe set
@ast
Molecular definition of high-r ...... nchored FISH banding probe set
@en
Molecular definition of high-r ...... chored FISH banding probe set.
@nl
type
label
Molecular definition of high-r ...... nchored FISH banding probe set
@ast
Molecular definition of high-r ...... nchored FISH banding probe set
@en
Molecular definition of high-r ...... chored FISH banding probe set.
@nl
prefLabel
Molecular definition of high-r ...... nchored FISH banding probe set
@ast
Molecular definition of high-r ...... nchored FISH banding probe set
@en
Molecular definition of high-r ...... chored FISH banding probe set.
@nl
P2093
P2860
P356
P1476
Molecular definition of high-r ...... nchored FISH banding probe set
@en
P2093
Anja Weise
Ina Fickelscher
Kristin Mrasek
Nadezda Kosyakova
Sau Wai Cheung
Thomas Liehr
Uwe Claussen
Wei Wen Cai
P2860
P304
P356
10.1369/JHC.2008.950550
P577
2008-02-05T00:00:00Z