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Birth defects

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

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Celebrating Match Day 2019 at Baylor

From The Labs Image of the Month

From the Labs features an image of mouse lung fluorescent teal muscle defining smooth muscle cells in the trachea and arteries. Learn more.

Celebrating Diversity at Baylor College of Medicine

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