Published in
Wiley, Birth Defects Research Part A: Clinical and Molecular Teratology, 1(106), p. 61-68, 2015
DOI: 10.1002/bdra.23463
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Variability in a three-generation family with pierre robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9 , and including KCNJ2 and KCNJ16
Journal article published in 2015 by
A. Polimeni,
A. Pizzuti,
A. Silvestri,
M. Roggini,
L. Tarani,
Marco Castori,
P. Papoff,
G. S. Sforzolini,
Irene Bottillo,
Silvia Morlino,
Chiara Barone,
Piero Cascone,
Paola Grammatico,
Luigi Laino,
A. Giancotti 
and other authors.
and other authors.
This paper is available in a repository.
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