Publications:

A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.

International Journal Of Pediatric Otorhinolaryngology

Widdershoven, Josine C C JC; Bowser, Mark M; Sheridan, Molly B MB; McDonald-McGinn, Donna M DM; Zackai, Elaine H EH; Solot, Cynthia B CB; Kirschner, Richard E RE; Beemer, Frits A FA; Morrow, Bernice E BE; Devoto, Marcella M; Emanuel, Beverly S BS

Publication Date: 2013-01

Variant appearance in text: rs4673309

PubMed Link: 23121717

Variant Present in the following documents:

• Main text

View BVdb publication page