(Q36683045)

English

Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish

scientific article published on 25 October 2012

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Europe PubMed Central

PMC publication ID

15 August 2017

Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish (English)

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Europe PubMed Central

PMC publication ID

15 August 2017

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Christopher J. Mungall

3

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

Barbara J. Ruef

5

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Europe PubMed Central

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15 August 2017

12

object named as

Peter N Robinson

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7

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Damian Smedley

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15 August 2017

Cynthia L Smith

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Cynthia Smith

6

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Sebastian Köhler

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Sebastian Köhler

2

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Eva Klopocki

9

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Georgios V. Gkoutos

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Georgios V Gkoutos

4

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13

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Suzanna E Lewis

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15 August 2017

Sebastian Bauer

8

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Sebastian Bauer

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Europe PubMed Central

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15 August 2017

Paul N. Schofield

10

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Paul N Schofield

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Europe PubMed Central

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15 August 2017

author name string

Sandra C Doelken

1

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Europe PubMed Central

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15 August 2017

Monte Westerfield

11

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Europe PubMed Central

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15 August 2017

publication date

25 October 2012

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Europe PubMed Central

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15 August 2017

number of pages

15

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Disease Models & Mechanisms

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Europe PubMed Central

PMC publication ID

15 August 2017

6

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Europe PubMed Central

PMC publication ID

15 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

358-372

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Europe PubMed Central

PMC publication ID

15 August 2017

copyright license

Creative Commons Attribution 2.0 Generic

18 May 2021

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April 2022 Public Data File from Crossref

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describes a project that uses

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Europe PubMed Central

9 June 2022

https://europepmc.org/search?query=(METHODS:'Cytoscape')

based on heuristic

inferred from PubMed Central ID database lookup

Computational tools for comparative phenomics: the role and promise of ontologies

1 reference

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Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium

1 reference

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Mouse genetic and phenotypic resources for human genetics

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1 reference

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1 reference

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ZFIN: enhancements and updates to the Zebrafish Model Organism Database

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Phenotype ontologies for mouse and man: bridging the semantic gap.

1 reference

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Accurate distinction of pathogenic from benign CNVs in mental retardation

1 reference

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Williams-Beuren syndrome.

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30 September 2017

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Forging links between human mental retardation-associated CNVs and mouse gene knockout models

1 reference

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DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

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1 reference

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Template Switching: From Replication Fork Repair to Genome Rearrangements

1 reference

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1242/DMM.010322

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

15 August 2017

ResearchGate publication ID

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