Search

Your search keyword '"Jones, L.J."' showing total 37 results

Search Constraints

Start Over You searched for: Author "Jones, L.J." Remove constraint Author: "Jones, L.J."
37 results on '"Jones, L.J."'

Search Results

1. A gene pathogenicity tool “GenePy” identifies missed biallelic diagnoses in the 100,000 Genomes Project

2. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

3. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

4. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

5. Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

6. A gene pathogenicity tool “GenePy” identifies missed biallelic diagnoses in the 100,000 Genomes Project

7. Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies

8. Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish

9. Heterozygous lamin B1 and lamin B2 variants cause primary microcephaly and define a novel laminopathy

10. DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration

11. Biallelic CRELD1 variants cause a multisystem syndrome including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.

12. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

13. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

14. Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

15. Heterozygous UCHL1 loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy

16. Expanding SPTAN1monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia

17. Heterozygous UCHL1loss-of-function variants cause a neurodegenerative disorder with spasticity, ataxia, neuropathy, and optic atrophy

18. Biallelic variants in KARS1are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish

21. Biallelic CRELD1variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

22. Dexmedetomidine for analgesia and sedation in newborn infants receiving mechanical ventilation.

26. Stability of the Oil-Air Boundary in Fluid Dynamic Bearings of Hard Disk Drives

30. Selective and Rapid Biosensor Integrated into a Commercial Hand‐Held Instrument for the Measurement of Ammonium Ion in Sewage Effluent.

31. 'Thus the Colliers and their wives…' * : migration, mate choice and population structure of some County Durham parishes in the mid-19th century.

34. Canola use in juvenile chinook salmon diets

Catalog

Books, media, physical & digital resources