Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male - Wikidata - awgldk - TriplyDB

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

http://www.wikidata.org/entity/Q30491459

about

A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity.Ring chromosome 10: report on two patients and review of the literature.Clinical impact of proximal autosomal imbalances.

P2860

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P2860

Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male

http://www.wikidata.org/entity/Q30491459

description

2009 nî lūn-bûn

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2009 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2009 թվականի հունվարին հրատարակված գիտական հոդված

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2009年の論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年論文

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2009年论文

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name

Characterization of a prenatal ...... n a phenotypically normal male

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Characterization of a prenatal ...... n a phenotypically normal male

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Characterization of a prenatal ...... n a phenotypically normal male

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Characterization of a prenatal ...... n a phenotypically normal male

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Characterization of a prenatal ...... n a phenotypically normal male

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Characterization of a prenatal ...... n a phenotypically normal male

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Molecular Cytogenetics

P1476

Characterization of a prenatal ...... n a phenotypically normal male

@en

P2093

Aikaterini Metaxotou

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Anja Weise

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Antonios Garas

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Elisabeth Ewers

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Emmanouil Manolakos

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Magdalini Lagou

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Maria Kontodiou

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Nadezda Kosyakova

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Sofia Kitsiou-Tzeli

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Thomas Liehr

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P2860

Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.

Identification of supernumerary marker chromosomes derived from chromosomes 5, 6, 19, and 20 using FISH.

Directly transmitted unbalanced chromosome abnormalities and euchromatic variants

Small supernumerary marker chromosomes (sSMC) in humans.

Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).

A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).

Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis.

An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line.

Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.

Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics.

P2888

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10.1186/1755-8166-2-1

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