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. Franca, Erica H. Gerkes, Dorothy K. Grange, Donald W. Hadley, Jarmo Jaaskelainen, Sabrina S. Paulo, Patrick Rump, Constantine A. Stratakis, Elizabeth M. Thompson, Mary Willis, Thomas L. Winder, Alexander A. L. Jorge, Erich Roessler, Maximilian Muenke*

*Corresponding author for this work

    Research output: Contribution to journal › Article › Academic › peer-review

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    Biochemistry, Genetics and Molecular Biology

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