Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly

Kelly A. Bear, Benjamin D. Solomon, Sonir Antonini, Ivo J.P. Arnhold, Marcela M. França, Erica H. Gerkes, Dorothy K. Grange, Donald W. Hadley, Jarmo Jääskeläinen, Sabrina S. Paulo, Patrick Rump, Constantine A. Stratakis, Elizabeth M. Thompson, Mary Willis, Thomas L. Winder, Alexander A.L. Jorge, Erich Roessler, Maximilian Muenke

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Fingerprint

Dive into the research topics of 'Pathogenic mutations in GLI2 cause a specific phenotype that is distinct from holoprosencephaly'. Together they form a unique fingerprint.

Medicine & Life Sciences