Christine Bellanné-Chantelot
Assistance Publique-Hôpitaux de Paris (AP-HP) Saint-Antoine
Department of Cytogenetics
Paris
France
Name/email consistency: high
- Genetic and clinical implications of the Val617Phe JAK2 mutation in 72 families with myeloproliferative disorders. Bellanné-Chantelot, C., Chaumarel, I., Labopin, M., Bellanger, F., Barbu, V., De Toma, C., Delhommeau, F., Casadevall, N., Vainchenker, W., Thomas, G., Najman, A. Blood (2006)
- Large genomic rearrangements in the hepatocyte nuclear factor-1beta (TCF2) gene are the most frequent cause of maturity-onset diabetes of the young type 5. Bellanné-Chantelot, C., Clauin, S., Chauveau, D., Collin, P., Daumont, M., Douillard, C., Dubois-Laforgue, D., Dusselier, L., Gautier, J.F., Jadoul, M., Laloi-Michelin, M., Jacquesson, L., Larger, E., Louis, J., Nicolino, M., Subra, J.F., Wilhem, J.M., Young, J., Velho, G., Timsit, J. Diabetes (2005)
- Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register. Bellanné-Chantelot, C., Clauin, S., Leblanc, T., Cassinat, B., Rodrigues-Lima, F., Beaufils, S., Vaury, C., Barkaoui, M., Fenneteau, O., Maier-Redelsperger, M., Chomienne, C., Donadieu, J. Blood (2004)
- Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations. Bellanné-Chantelot, C., Chauveau, D., Gautier, J.F., Dubois-Laforgue, D., Clauin, S., Beaufils, S., Wilhelm, J.M., Boitard, C., Noël, L.H., Velho, G., Timsit, J. Ann. Intern. Med. (2004)