Demographic history of India and mtDNA-sequence diversity.

Por Mountain, J L, Hebert, J M, Bhattacharyya, S, Underhill, P A, Ottolenghi, C, Gadgil, M, Cavalli-Sforza, L L
Publicado em 1995

P07.15 Diagnostic value of 2-hydroxyglutarate detection by 1H MR spectroscopy in patients with glioma and correlations with tumor phenotype and tissue dosage

Por Di Stefano, A. L., Branzoli, F., Ottolenghi, C., Capelle, L., Mokhtari, K., Villa, C. M., Giry, M., Marjanska, M., Lehericy, S., Sanson, M.
Publicado no Neuro Oncol (2016)

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

Por 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
Publicado em 2002

Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis

Por Habarou, F., Brassier, A., Rio, M., Chrétien, D., Monnot, S., Barbier, V., Barouki, R., Bonnefont, J.P., Boddaert, N., Chadefaux-Vekemans, B., Le Moyec, L., Bastin, J., Ottolenghi, C., de Lonlay, P.
Publicado no Mol Genet Metab Rep (2014)