Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH).
about
Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplificationFluorescence In situ Hybridization: Cell-Based Genetic Diagnostic and Research ApplicationsMLPAinter for MLPA interpretation: an integrated approach for the analysis, visualisation and data management of Multiplex Ligation-dependent Probe Amplification.Cytogenetic analysis in prenatal diagnosis.Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting.Rapid prenatal diagnosis of Down Syndrome using quantitative fluorescent PCR in uncultured amniocytes.Rapid screening for chromosomal aneuploidies using array-MLPA.Microfluidic digital PCR enables rapid prenatal diagnosis of fetal aneuploidyRapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization: clinical experience with 4,500 specimensChromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.Sex chromosome aneuploidies among men with systemic lupus erythematosus.Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization.Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal Abnormalities.Prenatal detection of chromosome aneuploidies in uncultured chorionic villus samples by FISHPaternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.Chromosomal localization of glutamate receptor genes: relationship to familial amyotrophic lateral sclerosis and other neurological disorders of mice and humans.A four-year retrospective study of amniocentesis: one centre experience.A prospective two years study of first trimester screening for Down syndromePrenatal detection of unbalanced chromosomal rearrangements by array CGH.Rapid-prenatal diagnosis through fluorescence in situ hybridization for preventing aneuploidy related birth defects.FISH detection of trisomy 21 in interphase by the simultaneous use of two differentially labelled cosmid contigs.Simultaneous, multilocus FISH analysis for detection of microdeletions in the diagnostic evaluation of developmental delay and mental retardation.Exclusive detection of the t(11;18)(q21;q21) in extranodal marginal zone B cell lymphomas (MZBL) of MALT type in contrast to other MZBL and extranodal large B cell lymphomas.Efficacy and applicability of interphase fluorescence in situ hybridization for prenatal diagnosis.
P2860
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P2860
Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH).
description
1992 nî lūn-bûn
@nan
1992 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Rapid detection of chromosome ...... in situ hybridization (FISH).
@ast
Rapid detection of chromosome ...... in situ hybridization (FISH).
@en
type
label
Rapid detection of chromosome ...... in situ hybridization (FISH).
@ast
Rapid detection of chromosome ...... in situ hybridization (FISH).
@en
prefLabel
Rapid detection of chromosome ...... in situ hybridization (FISH).
@ast
Rapid detection of chromosome ...... in situ hybridization (FISH).
@en
P2093
P2860
P1476
Rapid detection of chromosome ...... in situ hybridization (FISH).
@en
P2093
B Leverone
R Osathanondh
P2860
P407
P577
1992-07-01T00:00:00Z