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

2. Registered access: authorizing data access

4. Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland

5. Towards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms

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

7. Optimising diagnostic yield in highly penetrant genomic disease

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

10. 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.

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

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

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

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

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

18. Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

20. Roots of musicality: on neuro-musical thresholds and new evidence for bridges between musical expression and 'inner growth'

21. Registered access: authorizing data access

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

23. Towards robust clinical genome interpretation: developing a consistent terminology to characterize disease-gene relationships - allelic requirement, inheritance modes and disease mechanisms.

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