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CRKL

From The Labs

CRKL in 22q11.2; a key gene that contributes to common birth defects

May 24, 2017 Ana Rodríguez 0 Comments 22q11.2, Birth defects, CRKL, cryptorchidism, DiGeorge syndrome, Genetics, genitourinary birth defects, hypospadias, kidney birth defects, mouse model

The 22q11.2 region of human chromosome 22 is a hotspot for a variety of birth defects. Scientists learned about this

From the Labs features the diversity of adult-born neurons, which was detailed in a recent issue of Cell Reports. Image courtesy of the Arenkiel lab, Patrick Hunt and Cell Reports. Learn more.