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11 results on '"Perrett, Daniel"'

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1. Registered access: authorizing data access

2. Optimizing the Diagnosis of Rare Genomic Disease in the UK and Ireland

3. Prevalence and architecture of de novo mutations in developmental disorders

4. Your Child and Language, Reading, Writing. Getting Involved Workshop Guide: A Manual for the Parent Group Trainer. The Best of BES--Basic Educational Skills Materials.

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

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

7. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

8. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

9. Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

10. Toward robust clinical genome interpretation: Developing a consistent terminology to characterize Mendelian disease-gene relationships—allelic requirement, inheritance modes, and disease mechanisms

11. DECIPHER: Supporting the interpretation and sharing of rare disease phenotype-linked variant data to advance diagnosis and research

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