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FOXP1-related intellectual disability syndrome : a recognizable entity
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FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions
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Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals
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Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in Blepharophimosis syndrome