APA
Jeandidier E., Gervais C., Radford-Weiss I., Zink E., Gangneux C., Eischen A., Galoisy A. C., Helias C., Dano L., Cammarata O., Jung G., Harzallah I., Guérin E., Martzolff L., Drénou B., Lioure B., Tancrédi C., Rimelen V. & Mauvieux L. (20121009). A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity. : Cancer genetics.
Chicago
Jeandidier Eric, Gervais Carine, Radford-Weiss Isabelle, Zink Estelle, Gangneux Catherine, Eischen Alice, Galoisy Anne Cécile, Helias Catherine, Dano Laurent, Cammarata Ornella, Jung Georges, Harzallah Inès, Guérin Eric, Martzolff Lionel, Drénou Bernard, Lioure Bruno, Tancrédi Céline, Rimelen Valérie and Mauvieux Laurent. 20121009. A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity. : Cancer genetics.
Harvard
Jeandidier E., Gervais C., Radford-Weiss I., Zink E., Gangneux C., Eischen A., Galoisy A. C., Helias C., Dano L., Cammarata O., Jung G., Harzallah I., Guérin E., Martzolff L., Drénou B., Lioure B., Tancrédi C., Rimelen V. and Mauvieux L. (20121009). A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity. : Cancer genetics.
MLA
Jeandidier Eric, Gervais Carine, Radford-Weiss Isabelle, Zink Estelle, Gangneux Catherine, Eischen Alice, Galoisy Anne Cécile, Helias Catherine, Dano Laurent, Cammarata Ornella, Jung Georges, Harzallah Inès, Guérin Eric, Martzolff Lionel, Drénou Bernard, Lioure Bruno, Tancrédi Céline, Rimelen Valérie and Mauvieux Laurent. A cytogenetic study of 397 consecutive acute myeloid leukemia cases identified three with a t(7;21) associated with 5q abnormalities and exhibiting similar clinical and biological features, suggesting a new, rare acute myeloid leukemia entity. : Cancer genetics. 20121009.