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1. An Inquiry-Based In-Person or Remote Laboratory Using Iron Analysis and Paper Microfluidics to Teach Analytical Method Development

2. Determining the Locations of Dust Sources in FeLoBAL Quasars

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3. Mutational Analysis in X-Linked Spondyloepiphyseal Dysplasia Tarda1

4. Clinical genetics in neurological disease

5. Molecular basis of neurofibromatosis type 1 (NF1): Mutation analysis and polymorphisms in the NF1 gene

6. Developing a quality scoring system for epidemiological surveys of genetic disorders

8. A specific mutation for Huntington's disease

9. Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length

10. Dentatorubral and pallidoluysian atrophy (DRPLA). Clinical and neuropathological findings in genetically confirmed North American and European pedigrees

12. Editorial postscript: 10 years of change and evolution

13. Genetic testing for familial hypertrophic cardiomyopathy in newborn infants

15. Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD)

16. Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy

17. Motor neurone disease--a study of prevalence and disability

19. Cataract and myotonic dystrophy: the role of molecular diagnosis

20. Psychosocial genetics: an emerging scientific discipline

21. Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy

22. Advances in myotonic dystrophy: a clinical and genetic perspective

23. The mapping of chromosome 4q markers in relation to facioscapulohumeral muscular dystrophy (FSHD)

24. Anticipation in myotonic dystrophy: new light on an old problem

25. Anal abnormalities in childhood myotonic dystrophy--a possible source of confusion in child sexual abuse

26. The human genome project and medical genetics

27. Genetic counselling in facioscapulohumeral muscular dystrophy

28. Polycystic kidney disease re-evaluated: a population-based study

29. Delivery of genetic services

30. Genetics services in the community

31. Medical genetics in the UK and the National Health Service

32. Direct marketing of cystic fibrosis carrier screening: commercial push or population need?

33. Clinical consequences of isolating the gene for Huntington's disease

35. Sub-Nanometer Au Monolayer-Protected Clusters Exhibiting Molecule-like Electronic Behavior:  Quantitative High-Angle Annular Dark-Field Scanning Transmission Electron Microscopy and Electrochemical Characterization of Clusters with Precise...

38. 17. Regional mapping of the facioscapulohumeral muscular dystrophy gene on 4q35: linkage analysis of the International Consortium

40. Reproductive problems and neonatal loss in women with myotonic dystrophy

41. Molecular deletion analysis in Duchenne muscular dystrophy

42. Screening for Duchenne muscular dystrophy

43. Congenital myotonic dystrophy in Britain. I. Clinical aspects

44. Hereditary distal spinal muscular atrophy with vocal cord paralysis

45. Genetic markers in Welsh gypsies

46. The delivery of genetic counseling services in Europe

47. Medical genetics in China: a western view

48. Ichthyosis, hepatosplenomegaly, and cerebellar degeneration in a sibship

49. MR imaging of calcified intracranial lesions

50. Mild form of Hunter's syndrome: clinical delineation based on 31 cases