5 results on '"Yu, Yongguo"'
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2. 22q11.2 Microduplication in a patient with 19p13.12–13.13 deletion
3. Clinical and molecular genetic study of infantile-onset Pompe disease in Chinese patients: Identification of 6 novel mutations
4. Molecular defects identified by whole exome sequencing in a child with Fanconi anemia
5. A unique combination of 17pter trisomy and 21qter monosomy in a boy with developmental delay, severe intellectual disability, growth retardation and dysmorphisms
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