Published in
Wiley, The American Journal of Medical Genetics - Part A, 7(161), p. 1797-1802, 2013
DOI: 10.1002/ajmg.a.36054
Links
Tools
Contiguous gene deletion of TBX5 and TBX3 leads to a varible phenotype with combined features of holt-oram and ulnar-mammary syndromes
Journal article published in 2013 by
Caroline Alby,
Bettina Bessieres,
Eric Bieth,
Tania Attie-Bitach,
Laurent Fermont,
Isabelle Citony,
Ferechté Razavi,
Michel Vekemans,
Fabienne Escande,
Sylvie Manouvrier,
Valérie Malan,
Jeanne Amiel 
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 