Scimitar sign with normal pulmonary venous drainage and anomalous inferior vena cava.

door Herer, B, Jaubert, F, Delaisements, C, Huchon, G, Chretien, J
Gepubliceerd in 1988

Effects of inflammation and fibrosis on pulmonary function in diffuse lung fibrosis.

door Chinet, T, Jaubert, F, Dusser, D, Danel, C, Chrétien, J, Huchon, G J
Gepubliceerd in 1990

Study of immunoglobulins in pleura and pleural effusions.

door Telvi, L, Jaubert, F, Eyquem, A, Andreux, J P, Labrousse, F, Chrétien, J
Gepubliceerd in 1979

Familial case with sequence variant in the testis-determining region associated with two sex phenotypes.

door Vilain, E, McElreavey, K, Jaubert, F, Raymond, J P, Richaud, F, Fellous, M
Gepubliceerd in 1992

The ultrastructural aspects of neoplastic myoepithelial cell in pleomorphic adenomas of salivary glands

door Margaritescu, C., Raica, M., Florescu, Maria, Simionescu, Cristiana, Surpateanu, M., Jaubert, F., Bogdan, FI.
Gepubliceerd in J Cell Mol Med (2007)

Testicular dysgenesis does not affect expression of anti-müllerian hormone by Sertoli cells in premeiotic seminiferous tubules.

door Rey, R., al-Attar, L., Louis, F., Jaubert, F., Barbet, P., Nihoul-Fékété, C., Chaussain, J. L., Josso, N.
Gepubliceerd in 1996

Evolution and expression of FOXL2

door Cocquet, J, Pailhoux, E, Jaubert, F, Servel, N, Xia, X, Pannetier, M, De Baere, E, Messiaen, L, Cotinot, C, Fellous, M, Veitia, R
Gepubliceerd in 2002

Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locus

door de Pontual, L, Pelet, A, Trochet, D, Jaubert, F, Espinosa‐Parrilla, Y, Munnich, A, Brunet, J‐F, Goridis, C, Feingold, J, Lyonnet, S, Amiel, J
Gepubliceerd in 2006

Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses

door Vialard, F, Ottolenghi, C, Gonzales, M, Choiset, A, Girard, S, Siffroi, J, McElreavey, K, Vibert-Guigue, C, Sebaoun, M, Joye, N, Portnoi, M, Jaubert, F, Fellous, M
Gepubliceerd in 2002

Swyer syndrome and 46,XY partial gonadal dysgenesis associated with 9p deletions in the absence of monosomy-9p syndrome.

door Veitia, R A, Nunes, M, Quintana-Murci, L, Rappaport, R, Thibaud, E, Jaubert, F, Fellous, M, McElreavey, K, Gonçalves, J, Silva, M, Rodrigues, J C, Caspurro, M, Boieiro, F, Marques, R, Lavinha, J
Gepubliceerd in 1998

Congenital hyperinsulinism and mosaic abnormalities of the ploidy

door Giurgea, I, Sanlaville, D, Fournet, J‐C, Sempoux, C, Bellanné‐Chantelot, C, Touati, G, Hubert, L, Groos, M‐S, Brunelle, F, Rahier, J, Henquin, J‐C, Dunne, M J, Jaubert, F, Robert, J‐J, Nihoul‐Fékété, C, Vekemans, M, Junien, C, de Lonlay, P
Gepubliceerd in 2006