A Comprehensive Genotype–phenotype Evaluation of Eight Chinese Probands with Waardenburg Syndrome

Sijun Li,Mengyao Qin,Shuang Mao,Lingyun Mei,Xinzhang Cai,Yong Feng,Chufeng He,Jian Song

BMC Medical Genomics（2022）

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Key words
Waardenburg syndrome,Genotype,Phenotype,Inner ear malformation,Unilateral hearing loss,Heterochromia iridis
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