Concepedia

Publication | Open Access

Pathogenic mutations in <i>GLI2</i> cause a specific phenotype that is distinct from holoprosencephaly

DOIFull Paper Access

60

Citations

24

References

2014

Year

Kelly Bear, Benjamin D. Solomon, Sonir Roberto Rauber Antonini, Ivo J.P. Arnhold, Marcela M. França, Erica H. Gerkes, Dorothy K. Grange, Donald W. Hadley, Jarmo Jääskeläinen, Sabrina Soares Paulo,
Journal of Medical Genetics

Abstract

98-HG-0249/04-HG-0093.

References

YearCitations

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