Publications
Export 2 results:
Author Title [ Year] Filters: First Letter Of Title is T and Author is Witmer, P Dane [Clear All Filters]
Two novel germline DDX41 mutations in a family with inherited myelodysplasia/acute myeloid leukemia. Haematologica 101, e228-31 (2016).
Truncating mutations in the last exon of NOTCH3 cause lateral meningocele syndrome. Am J Med Genet A 167A, 271-81 (2015).