Search

Your search keyword '"Lahiri N"' showing total 146 results

Search Constraints

Start Over You searched for: Author "Lahiri N" Remove constraint Author: "Lahiri N"
146 results on '"Lahiri N"'

Search Results

1. Identification of markers of disease onset and progression in Huntington's Disease

2. PUF60‐related developmental disorder: A case series and phenotypic analysis of 10 additional patients with monoallelic PUF60 variants

3. PUF60-related developmental disorder:A case series and phenotypic analysis of 10 additional patients with monoallelic PUF60 variants

4. Combined multiplet theory and experiment for the Fe 2p and 3p XPS of FeO and Fe2O3.

5. Covalency in Fe2O3 and FeO: Consequences for XPS satellite intensity.

6. Analysis of the Fe 2p XPS for hematite α Fe2O3: Consequences of covalent bonding and orbital splittings on multiplet splittings.

10. Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes

11. Association of CAG Repeats With Long-term Progression in Huntington Disease

12. Origin of the complex main and satellite features in Fe 2p XPS of Fe2O3.

18. Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome

19. Identification of symbol digit modality test score extremes in Huntington's disease

20. Apathy associated with impaired recognition of happy facial expressions in Huntington's disease

21. 27 years of prenatal diagnosis for Huntington disease in the United Kingdom

22. MSH3 modifies somatic instability and disease severity in Huntington's and myotonic dystrophy type 1

23. Different mutations in DEAF1 lead to clinically distinct dominant and recessive forms of intellectual disability

24. De novo and biallelic DEAF1 variants cause a phenotypic spectrum

25. The phenotype of Sotos syndrome in adulthood: A review of 44 individuals

26. Predictive testing of minors for Huntington's disease: The UK and Netherlands experiences\ud

29. Suicidal ideation in a European Huntington's disease population

30. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

31. Commission des Ephemerides

32. Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

33. The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients

34. Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY

35. NMDA receptor gene variations as modifiers in Huntington disease: a replication study

36. β-Defensin Genomic Copy Number Does Not Influence the Age of Onset in Huntington's Disease

37. Is there a global small world of owners and directors?

38. Discrepancies in reporting the CAG repeat lengths for Huntington's disease

39. NMDA receptor gene variations as modifiers in Huntington disease

43. Archaeology and world religion. (Book Reviews: Archaeology)

Catalog

Books, media, physical & digital resources