Literature DB >> 25974718

GLI2 mutations typically result in pituitary anomalies with or without postaxial polydactyly.

Kelly A Bear1, Benjamin D Solomon2,3,4.   

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Year:  2015        PMID： 25974718     DOI： 10.1002/ajmg.a.37160

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  2 in total

1.  Molecular testing in holoprosencephaly.

Authors:  Paul Kruszka; Ariel F Martinez; Maximilian Muenke
Journal:  Am J Med Genet C Semin Med Genet       Date:  2018-05-17       Impact factor: 3.908

2.  A novel truncating variant of GLI2 associated with Culler-Jones syndrome impairs Hedgehog signalling.

Authors:  Fabiola Valenza; Davide Cittaro; Elia Stupka; Donatella Biancolini; Maria Grazia Patricelli; Dario Bonanomi; Dejan Lazarević
Journal:  PLoS One       Date:  2019-01-10       Impact factor: 3.240
  2 in total

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