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Your search keyword '"Cilliers, Deirdre"' showing total 8 results

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8 results on '"Cilliers, Deirdre"'

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1. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

2. The contribution of X-linked coding variation to severe developmental disorders

3. Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing

4. Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study

5. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

6. Diagnosis of lethal or prenatal-onset autosomal recessive disorders by parental exome sequencing

7. Diagnostic value of exome and whole genome sequencing in craniosynostosis

8. Diagnosis of lethal or prenatal-onset autosomal recessive disorders by parental exome sequencing

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