Next Generation Sequencing (NGS) von DNA

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Deutsch

Bibliographic citation: In: 10.4119/BUPRAKTISCH-1119

Keyword: Humangenetik
Genanalyse

Event: Veröffentlichung

(where): Aachen

(who): Universitätsbibliothek der RWTH Aachen

(when): 2018

Creator: Eggermann, Thomas
Söllner, Lukas
Kurth, Ingo
Eggermann, Katja
Begemann, Matthias

DOI: 10.18154/RWTH-2023-01872

URN: urn:nbn:de:101:1-2023030300402365678816

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 AM CEST

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Associated

Eggermann, Thomas
Söllner, Lukas
Kurth, Ingo
Eggermann, Katja
Begemann, Matthias
Universitätsbibliothek der RWTH Aachen

Time of origin

2018

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Next Generation Sequencing (NGS) von DNA

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Other Objects (12)

Next Generation Sequencing (NGS) von DNA : Mehr Informationen durch mehr Daten?

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Molecular mechanisms of human overgrowth and use of omics in its diagnostics : chances and challenges

Next Generation Sequencing (NGS)

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First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions

Cystinuria: an inborn cause of urolithiasis

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Next Generation Sequencing (NGS)

Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains

First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions

Cystinuria: an inborn cause of urolithiasis

Cystinuria : an inborn cause of urolithiasis

11p13 microduplication: a differential diagnosis of Silver–Russell syndrome?

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11p13 microduplication: a differential diagnosis of Silver–Russell syndrome?

Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domains

Next Generation Sequencing (NGS) von DNA : Mehr Informationen durch mehr Daten?

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

Molecular mechanisms of human overgrowth and use of omics in its diagnostics : chances and challenges

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Unusual deletion of the maternal 11p15 allele in Beckwith–Wiedemann syndrome with an impact on both imprinting domains

First-time application of droplet digital PCR for methylation testing of the 11p15.5 imprinting regions

Cystinuria: an inborn cause of urolithiasis

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