Imperial College London
Alternate

Dr Tony Goldstone

Faculty of Medicine, Department of Brain Sciences

Reader in PsychoNeuroEndocrinology
 
 
 
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Contact

 

+44 (0)20 7594 5989tony.goldstone Website

 
 
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Location

 

S25Commonwealth BuildingHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@inproceedings{Stutzmann:2009,
author = {Stutzmann, F and Ghoussaini, M and Couturier, C and Marchand, M and Vatin, V and Corset, L and Lecoeur, C and Balkau, B and Horber, F and Driscoll, DJ and Goldstone, AP and Weill, J and Michaud, JL and Meyre, D and Froguel, P},
pages = {S104--S104},
publisher = {SPRINGER},
title = {Loss-of-function mutations in SIM1 cause a specific form of Prader-Willi-like syndrome},
url = {https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000269262400239&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb},
year = {2009}
}
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RIS format (EndNote, RefMan)

TY  - CPAPER
AU  - Stutzmann,F
AU  - Ghoussaini,M
AU  - Couturier,C
AU  - Marchand,M
AU  - Vatin,V
AU  - Corset,L
AU  - Lecoeur,C
AU  - Balkau,B
AU  - Horber,F
AU  - Driscoll,DJ
AU  - Goldstone,AP
AU  - Weill,J
AU  - Michaud,JL
AU  - Meyre,D
AU  - Froguel,P
EP  - 104
PB  - SPRINGER
PY  - 2009///
SN  - 0012-186X
SP  - 104
TI  - Loss-of-function mutations in SIM1 cause a specific form of Prader-Willi-like syndrome
UR  - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000269262400239&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=a2bf6146997ec60c407a63945d4e92bb
ER  -
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