J. Chelly, Z. Tumer, and T. Tonnesen, Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein, Nat Genet, vol.3, pp.14-19, 1993.

M. F. Lyon, Gene action in the X-chromosome of the mouse (Mus musculus L.), Nature, vol.190, pp.372-373, 1961.

E. Beutler, M. Yeh, and V. F. Fairbanks, The normal human female as a mosaic of Xchromosome activity: studies using the gene for C-6-PD-deficiency as a marker, Proc. Natl. Acad. Sci. U.S.A, vol.48, pp.9-16, 1962.

H. Gruneberg, More about the tabby mouse and about the Lyon hypothesis, J. Embryol. Exp. Morph, vol.16, pp.569-590, 1966.

S. Augui and E. Heard,

, Med Sci (Paris), vol.24, pp.584-585, 2008.

L. Delaroche, P. Demailly, and K. Ancelin,

, Med Sci (Paris), vol.28, pp.526-530, 2012.

P. Navarro,

, Med Sci (Paris), vol.27, pp.476-479, 2011.

C. Rougeulle, X inactivation in embryonic stem cells is controlled by pluripotent genes

, Med Sci (Paris), vol.25, pp.234-235, 2009.

C. Vallot and C. Rougeulle, X chromosome inactivation in human: XACT and XIST, a non coding RNA for each X

, Med Sci (Paris), vol.29, pp.223-225, 2013.

C. Morey and P. Avner, The demoiselle of X-inactivation: 50 years old and as trendy and mesmerising as ever, PLoS Genet, vol.7, p.1002212, 2011.

M. F. Lyon and S. G. Hawkes, X-linked gene for testicular feminization in the mouse, Nature, vol.227, pp.1217-1219, 1970.

M. F. Lyon and S. Rastan, Genetic Variants and Strains of the Laboratory Mouse, 1996.