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22q11.2

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

May 24, 2017 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 region because it is deleted in

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From the Labs: Human retinal organoid.

Healthy Habits: A DOC-umentary Series

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