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Keze Ma

Boston Children's Hospital

7

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45

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A novel nonsense mutation of ZEB2 gene in a Chinese patient with Mowat-Wilson syndrome.

2020 Journal of Clinical Laboratory Analysis
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A novel homozygous initiation codon variant associated with infantile alpha‐Bcrystallinopathy in a Chinese family

2019 Molecular Genetics & Genomic Medicine
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A novel compound heterozygous mutation in VARS2 in a newborn with mitochondrial cardiomyopathy: a case report of a Chinese family

2018 BMC Medical Genetics
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Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns.

2016 Genetic Testing and Molecular Biomarkers
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Large Cohort Screening of G6PD Deficiency and the Mutational Spectrum in the Dongguan District in Southern China

2015 PLOS ONE
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Epidemiological investigation and risk factor analysis of childhood asthma in Dongguan area

2014 Chinese Journal of Applied Clinical Pediatrics
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