5 results on '"Li, Dongxiao"'
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2. Paternal uniparental disomy of chromosome 16 resulting in homozygosity of a GPT2 mutation causes intellectual and developmental disability
3. Eleven novel mutations and clinical characteristics in seven Chinese patients with thiamine metabolism dysfunction syndrome
4. Further delineation of AGPAT2 and BSCL2 related congenital generalized lipodystrophy in young infants
5. A chinese boy with geleophysic dysplasia caused by compound heterozygous mutations in ADAMTSL2
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