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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 journal › Article › peer-review
48
Scopus
citations