advertisement

---

Hanna C 1

Showing records 1 to 1 | Display all abstracts from Hanna C

96171 De novo PBX1 variant in a patient with glaucoma, kidney anomalies, and developmental delay: An expansion of the CAKUTHED phenotype
Safgren SL; Olson RJ; Pinto E Vairo F; Bothun ED; Hanna C; Klee EW; Schimmenti LA
American Journal of Medical Genetics, Part A 2022; 188: 919-925

---