AcroM fluorescent in situ hybridization analyses of marker chromosomes

No abstract is available for this paper.

• Publication year

  2001

• Venue

  Human Genetics

• Publication date

  2001-08-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s004390100571PMID 11511920
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Rapid generation of chromosome-specific alphoid DNA probes using the polymerase chain reaction

  2004cited by this paper
• Forty four probands with an additional “marker” chromosome

  2004cited by this paper
• Classifying by colors: FISH-based genome analysis

  2001cited by this paper
• Small Marker Chromosome Identification in Metaphase and Interphase Using Centromeric Multiplex FISH (CM-FISH)

  2001influential reference
• A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH)

  2001cited by this paper
• An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH.

  2000cited by this paper
• New strategy for multi-colour fluorescence in situ hybridisation: COBRA: COmbined Binary RAtio labelling

  1999cited by this paper
• Multiplex-FISH for pre- and postnatal diagnostic applications.

  1999cited by this paper
• Prenatal detection of extra structurally abnormal chromosomes (ESACs): new cases and a review of the literature

  1999cited by this paper
• Identification of de novo chromosomal markers and derivatives by spectral karyotyping

  1998influential reference
• An optimized, fully automated system for fast and accurate identification of chromosomal rearrangements by multiplex-FISH (M-FISH)

  1998cited by this paper
• FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases.

  1998influential reference
• A molecular and FISH approach to determining karyotype and phenotype correlations in six patients with supernumerary marker(22) chromosomes.

  1997cited by this paper
• Centromere DNA dynamics: latent centromeres and neocentromere formation.

  1997cited by this paper
• MICRODISSECTION AND DOP‐PCR‐BASED REVERSE CHROMOSOME PAINTING AS A FAST AND RELIABLE STRATEGY IN THE ANALYSIS OF VARIOUS STRUCTURAL CHROMOSOME ABNORMALITIES

  1996influential reference
• Karyotyping human chromosomes by combinatorial multi-fluor FISH

  1996cited by this paper
• Multicolor Spectral Karyotyping of Human Chromosomes

  1996cited by this paper
• Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.

  1995influential reference
• Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

  1994influential reference
• Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescence in situ hybridization

  1994influential reference
• Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization

  1993cited by this paper
• Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

  1993cited by this paper
• Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes

  1993cited by this paper
• A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

  1992influential reference
• A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH)

  1992cited by this paper
• Cytogenetic analysis by chromosome painting using dop‐pcr amplified flow‐sorted chromosomes

  1992influential reference
• Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.

  1992influential reference
• De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.

  1991influential reference
• Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

  1991cited by this paper
• Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.

  1990cited by this paper
• Complete human rDNA repeat units isolated in yeast artificial chromosomes.

  1989influential reference
• Bisatellited extra small metacentric chromosome in newborns

  1974cited by this paper

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  2021cites this paper
• New Sight on Assessment of Clinical Value of Human Supernumerary Marker Chromosomes

  2020cites this paper
• Chapter 14 – Molecular Cytogenetics in Molecular Diagnostics

  2017cites this paper
• Tetrasomy 9p Syndrome

  2016cites this paper
• Microdissection and Chromosome Painting

  2015cites this paper
• Molekulárne cytogenetická analýza marker chromozómov a príbuzných abnormalít

  2011influential citation
• Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8,18, and 21 in three patients

  2010cites this paper
• Molecular Cytogenetics in Molecular Diagnostics

  2010cites this paper
• Caractérisation de 10 marqueurs chromosomiques surnuméraires (MCS) : apport de l'hybridation génomique comparative sur microréseau (CHG-ARRAY)

  2010cites this paper
• Chromosome abnormalities without phenotypic consequences

  2010influential citation
• cenM-FISH Approaches

  2009cites this paper
• Fluorescence In Situ Hybridization (FISH) — Application Guide

  2009cites this paper
• [Strategies to identify supernumerary chromosomal markers in constitutional cytogenetics].

  2008cites this paper
• Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.

  2007cites this paper
• Prenatal diagnosis of nonmosaic tetrasomy 9p by microdissection and FISH: case report.

  2007cites this paper
• Personal information First name ( s ) / Surname ( s )

  2007cites this paper
• Aplicació de la citogenètica molecular a la genètica mèdica: malformacions congènites i infertilitat

  2007cites this paper
• Persistence of DNA threads in human anaphase cells suggests late completion of sister chromatid decatenation

  2007cites this paper
• Monitoring chromosome rearrangements.

  2005cites this paper
• M-FISH applications in clinical genetics.

  2005cites this paper
• New Developments in Multicolour Fluorescence in situ Hybridization

  2004cites this paper
• What Are B Chromosomes

  2004influential citation
• Multicolor FISH probe sets and their applications.

  2004cites this paper
• Human supernumeraries: are they B chromosomes?

  2004cites this paper
• Multicolor chromosome painting in diagnostic and research applications

  2004cites this paper
• Tetrasomy 21pter→q21.2 in a male infant without typical Down’s syndrome dysmorphic features but moderate mental retardation

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• SKY™ assessment of two karyotypes with 0–6 supernumerary marker/ring chromosomes and review of previously reported cases with two or more markers

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• Enlarged chromosome 13 p‐arm hiding a cryptic partial trisomy 6p22.2‐pter

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• Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification

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• Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis

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• Early amnioinfusion for anhydramnios after CVS

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• Multicolor FISH in two and three dimensions for clastogenic analyses.

  2002cites this paper
• Chromosomes Today

  1997cites this paper