9 results on '"Zeng, Shuhong"'
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2. A de novo PAK1 likely pathogenic variant and a de novo terminal 1q microdeletion in a Chinese girl with global developmental delay, severe intellectual disability, and seizures
3. Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview
4. Molecular cytogenetic analysis of partial monosomy 10p and trisomy 10q resulting from familial pericentric inversion (10): a first case report in Chinese population
5. Cytogenetic and molecular analysis of distal 4q duplication with distinctive phenotype using single-nucleotide polymorphism array
6. Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China
7. A prenatal diagnosis and genetics study of five pedigrees in the Chinese population with Xp22.31 microduplication
8. Molecular analysis of a large novel deletion causing α+-thalassemia.
9. Molecular analysis of a large novel deletion causing α + -thalassemia.
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