Published in
Elsevier, European Journal of Medical Genetics, 5(61), p. 248-252
DOI: 10.1016/j.ejmg.2017.12.008
Links
Tools
Refinement of the critical 7p22.1 deletion region: Haploinsufficiency of ACTB is the cause of the 7p22.1 microdeletion-related developmental disorders
Journal article published in 2018 by
Orazio Palumbo 
,
Maria Accadia,
Pietro Palumbo ,
Maria Pia Leone ,
Antonio Scorrano,
Teresa Palladino,
Raffaella Stallone,
Maria Clara Bonaglia ,
Massimo Carella
,
Maria Accadia,
Pietro Palumbo ,
Maria Pia Leone ,
Antonio Scorrano,
Teresa Palladino,
Raffaella Stallone,
Maria Clara Bonaglia ,
Massimo Carella
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 