Deletions of 9q21.3 including NTRK2 are associated with severe phenotype.

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

1552-4833

10.1002/ajmg.a.36797 doi


Abnormalities, Multiple--diagnosis
Chromosome Deletion
Chromosomes, Human, Pair 9
Female
Humans