Publication | Closed Access
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
305
Citations
21
References
1996
Year
Mendelian DisorderGenetic DisorderHomeobox Gene Emx2GeneticsPathogenesisPsychiatric GeneticsPathologyNeurogeneticsMolecular GeneticsDisease Gene IdentificationSevere SchizencephalyGermline MutationsMedicineClinical Genetics
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