6 results on '"Yang, Yanling"'
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2. Further delineation of AGPAT2 and BSCL2 related congenital generalized lipodystrophy in young infants
3. A chinese boy with geleophysic dysplasia caused by compound heterozygous mutations in ADAMTSL2
4. Seven novel mutations of the SMPD1 gene in four Chinese patients with Niemann-Pick disease type A and prenatal diagnosis for four fetuses
5. Eleven novel mutations of the BCKDHA, BCKDHB and DBT genes associated with maple syrup urine disease in the Chinese population: Report on eight cases
6. Very long-chain acyl-coenzyme A dehydrogenase deficiency in Chinese patients: Eight case reports, including one case of prenatal diagnosis
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