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

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: 11p13 microduplication: a differential diagnosis of Silver–Russell syndrome? ; volume:17 ; number:1 ; day:14 ; month:3 ; year:2024 ; pages:1-5 ; date:12.2024
Molecular cytogenetics ; 17, Heft 1 (14.3.2024), 1-5, 12.2024

Creator: Amin, Asmaa K.
Krause, Jeremias
Eggermann, Thomas

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13039-024-00672-6

URN: urn:nbn:de:101:1-2405162112592.612373673239

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 11:02 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Amin, Asmaa K.
Krause, Jeremias
Eggermann, Thomas
SpringerLink (Online service)

Other Objects (12)

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

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

Silver-Russell syndrome: genetic basis and molecular genetic testing

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

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

Kagami-Ogata syndrome : an important differential diagnosis to Beckwith-Wiedemann syndrome

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes

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

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

Silver-Russell syndrome: genetic basis and molecular genetic testing

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

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

Kagami-Ogata syndrome : an important differential diagnosis to Beckwith-Wiedemann syndrome

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes

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

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

Silver-Russell syndrome: genetic basis and molecular genetic testing

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

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

Kagami-Ogata syndrome : an important differential diagnosis to Beckwith-Wiedemann syndrome

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

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

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

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

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

Silver-Russell syndrome: genetic basis and molecular genetic testing

Silver-Russell syndrome: genetic basis and molecular genetic testing

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

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

Kagami-Ogata syndrome : an important differential diagnosis to Beckwith-Wiedemann syndrome

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes

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

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

Silver-Russell syndrome: genetic basis and molecular genetic testing

Silver-Russell syndrome: genetic basis and molecular genetic testing

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

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

Kagami-Ogata syndrome : an important differential diagnosis to Beckwith-Wiedemann syndrome

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes

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

Maternal Effect Mutations: A Novel Cause for Human Reproductive Failure

Silver-Russell syndrome: genetic basis and molecular genetic testing

Silver-Russell syndrome: genetic basis and molecular genetic testing

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

Novel mutation points to a hot spot in CDKN1C causing Silver–Russell syndrome

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

Kagami-Ogata syndrome : an important differential diagnosis to Beckwith-Wiedemann syndrome

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Microdeletions in 1q21 and 8q12.1 depict two additional molecular subgroups of Silver-Russell syndrome like phenotypes

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

Examinations of maternal uniparental disomy and epimutations for chromosomes 6, 14, 16 and 20 in Silver-Russell syndrome-like phenotypes

Related objects

Reset password