Hancarova, Miroslava Deletions of 9q21.3 including NTRK2 are associated with severe phenotype. [electronic resource] - American journal of medical genetics. Part A Jan 2015 - 264-7 p. digital Publication Type: Letter; Comment ISSN: 1552-4833 Standard No.: 10.1002/ajmg.a.36797 doi Subjects--Topical Terms: Abnormalities, Multiple--diagnosisChromosome DeletionChromosomes, Human, Pair 9FemaleHumans