A study on the clinical significance of the who aml subtype inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q chromosomal abnormalities in 6,819 aml cases

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Autoria(s): Lugthart S.; Groeschel S.; Beverloo H.; Valk P.; Schanz U.; Bhola S.; Vellenga E.; Kayser S.; Ossenkoppele G.; Verhoef G.; Ferrant A.; van den Berg-de Ruiter E.; Ganser A.; Jotterand M.; Krauter J.; Pabst T.; Schlegelberger B.; Schlenk R.; Delwel R.; Doehner K.; Loewenberg B.; Doehner H.

Data(s)	2010
Identificador	http://serval.unil.ch/?id=serval:BIB_644527E87B99 isbn:0390-6078 isiid:000279051301489
Idioma(s)	en
Fonte	15th Annual Meeting of the European Hematology Association
Tipo	info:eu-repo/semantics/conferenceObject inproceedings