
Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene
Keywords: OFC, occipitofrontal circumference; BERA, brainstem evoked response audiometry; aCGH, array comparative genomic hybridization; CNV, copy number variation; FISH, fluorescence in situ hybridization; ASD, autism spectrum disorder7q deletion; Comparative geno