Authors: Chen, Chun-An, Crutcher, Emeline, Gill, Harinder, Nelson, Tanya N, Robak, Laurie A, Jongmans, Marjolijn C J, Pfundt, Rolph, Prasad, Chitra, Berard, Roberta A, Fannemel, Madeleine, Frengen, Eirik, Misceo, Doriana, Ramsey, Keri, Yang, Yaping, Schaaf, Christian P, Wang, Xia
Superior Title: Paediatrics Publications
Subject Terms: CHDSKM, congenital heart defects, hearing impairment, renal hypoplasia, skeletal malformations, Pediatrics
Authors: Jordan, Valerie K., Fregeau, Brieana, Ge, Xiaoyan, Giordano, Jessica, Wapner, Ronald J., Balci, Tugce B., Carter, Melissa T., Bernat, John A., Moccia, Amanda N., Srivastava, Anshika, Martin, Donna M., Bielas, Stephanie L., Pappas, John, Svoboda, Melissa D., Rio, Marlène, Boddaert, Nathalie, Cantagrel, Vincent, Lewis, Andrea M., Scaglia, Fernando, Kohler, Jennefer N., Bernstein, Jonathan A., Dries, Annika M., Rosenfeld, Jill A., DeFilippo, Colette, Thorson, Willa, Yang, Yaping, Sherr, Elliott H., Bi, Weimin, Scott, Daryl A.
Superior Title: Paediatrics Publications
Subject Terms: 1p36 deletion syndrome, CHARGE syndrome, CHD7, genotype–phenotype correlations, NEDBEH, RERE
File Description: application/pdf
Relation: https://ir.lib.uwo.ca/paedpub/739; https://ir.lib.uwo.ca/context/paedpub/article/1747/viewcontent/humu23400_am.pdf