M. Tauber

CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome

A. Faussat, I. Netchine, S. Rossignol, 2013, Journal of Medical Genetics.

Russell Silver syndrome PCNA-binding domain as a cause of familial mutation affecting the CDKN 1 C

A. Faussat, I. Netchine, S. Rossignol, 2013 .

OBSL1 mutations in 3‐M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels

A. Munnich, H. Stewart, J. Michaud, 2010, Human mutation.

OBSL1 mutations in 3‐M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels

A. Munnich, H. Stewart, J. Michaud, 2010, Human mutation.