Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

L.T.J.N. van der Veken

Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

Translated title of the contribution: Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

L.T.J.N. van der Veken

Research output: Contribution to conference › Poster › Other research output

Translated title of the contribution	Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure
Original language	Undefined/Unknown
Publication status	Published - 6 Nov 2012
Event	American Society of Human Genetics - San Francisco USA Duration: 6 Nov 2012 → 10 Nov 2012

Conference

Conference	American Society of Human Genetics
City	San Francisco USA
Period	6/11/12 → 10/11/12

Cite this

@conference{5bf6b2833f284dc38f28a7ac4b0a11df,

title = "Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure",

author = "{van der Veken}, L.T.J.N.",

note = "American Society of Human Genetics; American Society of Human Genetics ; Conference date: 06-11-2012 Through 10-11-2012",

year = "2012",

month = nov,

day = "6",

language = "Undefined/Unknown",

}