Danesino, C.

mutation family patient deletion chromosome leukemia teeth chorea sequence protein study disorder disease analysis development oligodontia marker factor thyroid diagnosis v 617f mutation region myelomonocytic leukemia agenesi children genomic result university genet 200 control chromosomes department blood genetic myeloid npm 1 mutations myeloid leukemia chromosome 14 q chromosome 14 ptpn 11 movement family uk 1 member transcription basal function basal ganglia italy 9 mutations myelomonocytic individual missense pavia missense mutations primer 9 gene abnormality hematology /oncology university breedveld thyroid transcription factor event 11. myeloproliferative family nl 1 allele families nl 1 position blackwell publishing ltd hematopoietic g 713t hematology 1.2 mb range neuron al .10 kinase novel novel mutation genomic deletion identi fied pcr products