Familial Deafness, Congenital Heart Defects, and Posterior Embryotoxon Caused by Cysteine Substitution in the First Epidermal-Growth-Factor–Like Domain of Jagged 1

بواسطة Le Caignec, C., Lefevre, M., Schott, J. J., Chaventre, A., Gayet, M., Calais, C., Moisan, J. P.
منشور في 2002

Mapping of quantitative trait loci for blood pressure and cardiac mass in the rat by genome scanning of recombinant inbred strains.

بواسطة Pravenec, M, Gauguier, D, Schott, J J, Buard, J, Kren, V, Bila, V, Szpirer, C, Szpirer, J, Wang, J M, Huang, H
منشور في 1995

Valvular dystrophy associated filamin A mutations reveal a new role of its first repeats in small-GTPase regulation

بواسطة Duval, D., Lardeux, A., Le Tourneau, T., Norris, R.A., Markwald, R.R., Sauzeau, V., Probst, V., Le Marec, H., Levine, R., Schott, J.J., Merot, J.
منشور في 2013

Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.

بواسطة Kyndt, F, Schott, J J, Trochu, J N, Baranger, F, Herbert, O, Scott, V, Fressinaud, E, David, A, Moisan, J P, Bouhour, J B, Le Marec, H, Bénichou, B
منشور في 1998

The Bjornstad syndrome (sensorineural hearing loss and pili torti) disease gene maps to chromosome 2q34-36.

بواسطة Lubianca Neto, J F, Lu, L, Eavey, R D, Flores, M A, Caldera, R M, Sangwatanaroj, S, Schott, J J, McDonough, B, Santos, J I, Seidman, C E, Seidman, J G
منشور في 1998