DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
LinksClose Window
References
Klammt J, Kiess W, Pfäffle R.
IGF1R mutations as cause of SGA.
Best Pract Res Clin Endocrinol Metab 2011;
25 (01) 191-206
We do not assume any responsibility for the contents of the web pages of other providers.