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2. [Clinical and genetic analysis of three children patients with Kleefstra syndrome].
3. [Genetic analysis of three patients with Kleefstra syndrome].
4. Prenatal diagnosis of a female fetus with ring chromosome 9, 46,XX,r(9)(p24q34), and a de novo interstitial 9p deletion.
5. Genotype-phenotype correlations in a fetus with Kleefstra syndrome.
6. Homozygous 22q11.2 distal type II microdeletion is associated with syndromic neurodevelopmental delay.
7. Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals.
8. First episode of psychosis in Kleefstra syndrome: a case report.
9. Refining the 9q34.3 microduplication syndrome reveals mild neurodevelopmental features associated with a distinct global DNA methylation profile.
10. [Analysis of genetics mechanism for the phenotypic diversity in a patient carrying a rare ring chromosome 9].