Constitutional RUNX1 deletion presenting as non-syndromic thrombocytopenia with myelodysplasia: 21q22 ITSN1 as a candidate gene in mental retardation.
暂无分享,去创建一个
E. van Binsbergen | M. Poot | M. Ausems | A. Buijs | M. Bierings | S. N. van der Crabben | Saskia van der Crabben