Fig. 5From: Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case reportOligonucleotides array profile of our patients shows 1p36.32 deletion of 2,3 Mb. OMIM genes disease-causing inside the critical region 1p36.32, according UCSC: PEX10, PRDM16, CEP104Back to article page