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Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation
Saskia van der Crabben, Ellen van Binsbergen, Margreet Ausems, Martin Poot, Marc Bierings, Arjan BuijsVolume:
34
Year:
2010
Language:
english
Pages:
1
DOI:
10.1016/j.leukres.2009.06.030
File:
PDF, 536 KB
english, 2010