Multiplex-FISH for pre- and postnatal diagnostic applications. - Wikidata - awgldk - TriplyDB

Multiplex-FISH for pre- and postnatal diagnostic applications.

Multiplex-FISH for pre- and postnatal diagnostic applications.

http://www.wikidata.org/entity/Q34390002

about

Sequential application of interphase-FISH and CGH to single cells.A review of fluorescence in situ hybridization (FISH): current status and future prospects.Detection of chromosomal aberrations by a whole-genome microsatellite screen Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH.Radiation-induced chromosome aberrations: insights gained from biophysical modeling.American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation.Telomeres: a diagnosis at the end of the chromosomes Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods Copy number variant analysis of human embryonic stem cells.Characterisation of supernumerary chromosomal markers: a study of 13 cases.Identification of de novo chromosome rearrangements: five cases analyzed with differential chromosome painting.Subtelomeric rearrangements detected in patients with idiopathic mental retardation.New concepts to improve resolution and sensitivity of molecular cytogenetic diagnostics by multicolor fluorescence in situ hybridization.Small marker chromosome identification in metaphase and interphase using centromeric multiplex fish (CM-FISH).A classification efficiency test of spectral karyotyping and multiplex fluorescence in situ hybridization: identification of chromosome homologies between Homo sapiens and Hylobates leucogenys.Limitations of chromosome classification by multicolor karyotyping.Genetics 101: cytogenetics and FISH.Analysis of chromosomal alterations in non-small cell lung cancer by multiplex-FISH, comparative genomic hybridization, and multicolor bar coding.Twenty-four-color spectral karyotyping reveals chromosome aberrations in cytogenetically normal acute myeloid leukemia.A multicolor FISH assay does not detect DUP25 in control individuals or in reported positive control cells.Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis.Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype.Usefulness of high-resolution comparative genomic hybridization (CGH) for detecting and characterizing constitutional chromosome abnormalities.Multicolor karyotypic interpretation of a heterochromatin-associated marker chromosome in a dysmorphic girl with developmental delay.Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatin Detection of diagnostically critical, often hidden, anomalies in complex karyotypes of haematological disorders using multicolour fluorescence in situ hybridization

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Multiplex-FISH for pre- and postnatal diagnostic applications.

http://www.wikidata.org/entity/Q34390002

description

1999 nî lūn-bûn

@nan

1999 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1999 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1999年の論文

@ja

1999年論文

@yue

1999年論文

@zh-hant

1999年論文

@zh-hk

1999年論文

@zh-mo

1999年論文

@zh-tw

1999年论文

@wuu

name

Multiplex-FISH for pre- and postnatal diagnostic applications.

@ast

Multiplex-FISH for pre- and postnatal diagnostic applications.

@en

Multiplex-FISH for pre- and postnatal diagnostic applications.

@nl

type

label

Multiplex-FISH for pre- and postnatal diagnostic applications.

@ast

Multiplex-FISH for pre- and postnatal diagnostic applications.

@en

Multiplex-FISH for pre- and postnatal diagnostic applications.

@nl

prefLabel

Multiplex-FISH for pre- and postnatal diagnostic applications.

@ast

Multiplex-FISH for pre- and postnatal diagnostic applications.

@en

Multiplex-FISH for pre- and postnatal diagnostic applications.

@nl

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P1433

American Journal of Human Genetics

P1476

Multiplex-FISH for pre- and postnatal diagnostic applications.

@en

P2093

Apacik C

http://www.w3.org/2001/XMLSchema#string

Cohen M

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Cremer T

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Daumer-Haas C

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Fauth C

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Murken J

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Müller-Navia J

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Schuffenhauer S

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Uhrig S

http://www.w3.org/2001/XMLSchema#string

Wirtz A

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P2860

Multicolor Spectral Karyotyping of Human Chromosomes

Cytogenetic analysis by chromosome painting using DOP-PCR amplified flow-sorted chromosomes.

Metaphase and interphase cytogenetics with Alu-PCR-amplified yeast artificial chromosome clones containing the BCR gene and the protooncogenes c-raf-1, c-fms, and c-erbB-2.

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

Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16

Chromosomal in situ suppression hybridization of human gonosomes and autosomes and its use in clinical cytogenetics.

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

Minireview: cryptic translocations and telomere integrity

Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probes.

Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones.

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448-462

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scholarly article

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10.1086/302508

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2

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65

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Michael R. Speicher

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1999-08-01T00:00:00Z

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12882825

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10417288

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1377944

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