Prediction of outcome by prenatal Doppler analysis in a patient with aortic stenosis.

Por Jouk, P S, Rambaud, P
Publicado em 1991

Disabilities and trends over time in a French county, 1980–91

Por Cans, C, Guillem, P, Fauconnier, J, Rambaud, P, Jouk, P
Publicado em 2003

Fetal lung volume in congenital diaphragmatic hernia

Por Bonfils, M, Emeriaud, G, Durand, C, Brancato, S, Nugues, F, Jouk, P‐S, Wroblewski, I, Debillon, T
Publicado em 2006

A heterozygous endothelin 3 mutation in Waardenburg-Hirschsprung disease: is there a dosage effect of EDN3/EDNRB gene mutations on neurocristopathy phenotypes?

Por PINGAULT, V., BONDURAND, N., LEMORT, N., SANCANDI, M., CECCHERINI, I., HUGOT, J., JOUK, P., GOOSSENS, M.
Publicado em 2001

Currarino Syndrome and HPE Microform Associated with a 2.7-Mb Deletion in 7q36.3 Excluding SHH Gene

Por Coutton, C., Poreau, B., Devillard, F., Durand, C., Odent, S., Rozel, C., Vieville, G., Amblard, F., Jouk, P.-S., Satre, V.
Publicado em 2014

Characterization of a germline mosaicism in families with Lowe syndrome, and identification of seven novel mutations in the OCRL1 gene.

Por Satre, V, Monnier, N, Berthoin, F, Ayuso, C, Joannard, A, Jouk, P S, Lopez-Pajares, I, Megabarne, A, Philippe, H J, Plauchu, H, Torres, M L, Lunardi, J
Publicado em 1999