Imperial College London

DrAngharadRoberts

Faculty of MedicineNational Heart & Lung Institute

Clinical Senior Lecturer in Cardiovascular Genetics
 
 
 
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Contact

 

+44 (0)20 3313 8313angharad.roberts Website

 
 
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Location

 

Cardiovascular Genetics and GenomicsSydney StreetRoyal Brompton Campus

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Summary

 

Publications

Citation

BibTex format

@article{Barber:2013:10.1038/ejhg.2012.144,
author = {Barber, JCK and Hall, V and Maloney, VK and Huang, S and Roberts, AM and Brady, AF and Foulds, N and Bewes, B and Volleth, M and Liehr, T and Mehnert, K and Bateman, M and White, H},
doi = {10.1038/ejhg.2012.144},
journal = {EUROPEAN JOURNAL OF HUMAN GENETICS},
pages = {182--189},
title = {16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2},
url = {http://dx.doi.org/10.1038/ejhg.2012.144},
volume = {21},
year = {2013}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AU - Barber,JCK
AU - Hall,V
AU - Maloney,VK
AU - Huang,S
AU - Roberts,AM
AU - Brady,AF
AU - Foulds,N
AU - Bewes,B
AU - Volleth,M
AU - Liehr,T
AU - Mehnert,K
AU - Bateman,M
AU - White,H
DO - 10.1038/ejhg.2012.144
EP - 189
PY - 2013///
SN - 1018-4813
SP - 182
TI - 16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2
T2 - EUROPEAN JOURNAL OF HUMAN GENETICS
UR - http://dx.doi.org/10.1038/ejhg.2012.144
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000314003300008&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
VL - 21
ER -