Search

Your search keyword '"Perrett, Daniel"' showing total 20 results

Search Constraints

Start Over You searched for: Author "Perrett, Daniel" Remove constraint Author: "Perrett, Daniel" Publication Year Range Last 10 years Remove constraint Publication Year Range: Last 10 years
20 results on '"Perrett, Daniel"'

Search Results

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

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

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

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

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

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

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

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

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

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

Catalog

Books, media, physical & digital resources