(Q42245090)

19 October 2017

Copy number variation and susceptibility to complex traits (English)

1 reference

19 October 2017

1 reference

2

Katherina Walz

1 reference

19 October 2017

Cesar P Canales

1

1 reference

19 October 2017

23 December 2010

1 reference

19 October 2017

EMBO Molecular Medicine

1 reference

19 October 2017

3

1 reference

19 October 2017

1

1 reference

19 October 2017

1-4

1 reference

Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models

19 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

Phenotypic variability and genetic susceptibility to genomic disorders

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

Origins and functional impact of copy number variation in the human genome

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

Copy number variation in human health, disease, and evolution

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

Diet and the evolution of human amylase gene copy number variation

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

26 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3401997

Sensitized phenotypic screening identifies gene dosage sensitive region on chromosome 11 that predisposes to disease in mice

27 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1002%2FEMMM.201000111

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21204264

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1002/EMMM.201000111

1 reference

19 October 2017

1 reference

PMC publication ID

3401997

19 October 2017

PubMed publication ID

21204264

1 reference

PMC publication ID

3401997