(Q37585864)

English

The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2.

scientific article published on 17 July 2013

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

21 August 2017

The strength of combined cytogenetic and mate-pair sequencing techniques illustrated by a germline chromothripsis rearrangement involving FOXP2. (English)

1 reference

Europe PubMed Central

21 August 2017

12

object named as

Niels Tommerup

0 references

author name string

Lusine Nazaryan

1

1 reference

Europe PubMed Central

21 August 2017

Eunice G Stefanou

2

1 reference

Europe PubMed Central

21 August 2017

Claus Hansen

3

1 reference

Europe PubMed Central

21 August 2017

Nadezda Kosyakova

4

1 reference

Europe PubMed Central

21 August 2017

Mads Bak

5

1 reference

Europe PubMed Central

21 August 2017

Freddie H Sharkey

6

1 reference

Europe PubMed Central

21 August 2017

Theodora Mantziou

7

1 reference

Europe PubMed Central

21 August 2017

Anastasios D Papanastasiou

8

1 reference

Europe PubMed Central

21 August 2017

Voula Velissariou

9

1 reference

Europe PubMed Central

21 August 2017

Thomas Liehr

10

1 reference

Europe PubMed Central

21 August 2017

Maria Syrrou

11

1 reference

Europe PubMed Central

21 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

17 July 2013

1 reference

Europe PubMed Central

21 August 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

21 August 2017

22

1 reference

Europe PubMed Central

21 August 2017

338-343

1 reference

Europe PubMed Central

21 August 2017

3

1 reference

Europe PubMed Central

21 August 2017

copyright license

Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

17 July 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

https://scigraph.springernature.com/pub.10.1038/ejhg.2013.147

0 references

Disruption of a large intergenic noncoding RNA in subjects with neurodevelopmental disabilities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Diacylglycerol kinase β knockout mice exhibit attention-deficit behavior and an abnormal response on methylphenidate-induced hyperactivity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Complex reorganization and predominant non-homologous repair following chromosomal breakage in karyotypically balanced germline rearrangements and transgenic integration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Chromothripsis is a common mechanism driving genomic rearrangements in primary and metastatic colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

SVDetect: a tool to identify genomic structural variations from paired-end and mate-pair sequencing data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Fast and accurate long-read alignment with Burrows-Wheeler transform

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Human-specific transcriptional regulation of CNS development genes by FOXP2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Complex human chromosomal and genomic rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

FOXP2 as a molecular window into speech and language

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

The human genome browser at UCSC

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Molecular analysis of a complex chromosomal rearrangement and a review of familial cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Molecular cloning and expression of a 90-kDa diacylglycerol kinase that predominantly localizes in neurons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

23 August 2017

Cadherins and neuropsychiatric disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

6 September 2017

DNA breaks and chromosome pulverization from errors in mitosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

6 September 2017

Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

6 September 2017

Application of molecular cytogenetic techniques to clarify apparently balanced complex chromosomal rearrangements in two patients with an abnormal phenotype: case report

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

25 June 2018

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

25 June 2018

Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

1 September 2018

Expression of two type II cadherins, Cdh12 and Cdh22 in the developing and adult mouse brain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

1 September 2018

A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3925275

1 September 2018

Complex rearrangements between chromosomes 6, 10, and 11 with multiple deletions at breakpoints

1 reference

https://pubmed.ncbi.nlm.nih.gov/23860044

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/EJHG.2013.147

1 reference

Europe PubMed Central

21 August 2017

1 reference

Europe PubMed Central

21 August 2017

1 reference

Europe PubMed Central

21 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37585864&oldid=1864397882"