Search

Your search keyword '"Baty, David"' showing total 33 results

Search Constraints

Start Over You searched for: Author "Baty, David" Remove constraint Author: "Baty, David"
33 results on '"Baty, David"'

Search Results

1. Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing

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

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

5. Continuing the sequence? Towards an economic evaluation of whole genome sequencing for the diagnosis of rare diseases in Scotland

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

8. Linking employee policies to new forms of value creation: the challenge for organisations is to work harder to demonstrate the link between employment policies, practice and value creation

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

14. Better doubling for ultrafast lasers; frequency doubling of ultrafast laser pulses makes extra demands on nonlinear optical crystals

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

16. Sustaining value through people: a new report explores how businesses can develop their approach to their people to generate sustainable value for all stakeholders

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

19. The p.Glu477Lys Mutation in Keratin 5 Is Strongly Associated with Mortality in Generalized Severe Epidermolysis Bullosa Simplex

29. A technique for achieving prerestorative minor tooth movement with orthodontic separators

31. Ferrocement.

32. The application of MAPH, MLPA, Real-time PCR, and QF PACR in the routine diagnostic service, to determine gene dosage.

33. Chromosomal changes in colorectal adenomas: relationship to gene mutations and potential for clinical utility.

Catalog

Books, media, physical & digital resources