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1. Suggestion of linkage of a major locus for nonsyndromic orofacial cleft with F13A and tentative assignment to chromosome 6

2. A Systematic Single Nucleotide Polymorphism Screen to Fine-Map Alcohol Dependence Genes on Chromosome 7 Identifies Association With a Novel Susceptibility Gene ACN9

3. The adducted thumbs syndrome

4. Linkage analysis in von Willebrand disease

5. Genome Screen for Quantitative Trait Loci Underlying Normal Variation in Femoral Structure

6. Subtle changes among presymptomatic carriers of the Huntington's disease gene

7. Genome Screen for QTLs Contributing to Normal Variation in Bone Mineral Density and Osteoporosis*

8. Differences in duration of Huntington's disease based on age at onset

9. Description of the genetic analysis workshop 11 collaborative study on the genetics of alcoholism

10. No Genetic Effect of α1-Antichymotrypsin in Alzheimer Disease

11. Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension

12. Contributors and Participants

13. Huntington's disease research roster support with a microcomputer database management system

14. Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19

15. Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families

16. Fine Mapping of the Chromosome 12 Late-Onset Alzheimer Disease Locus: Potential Genetic and Phenotypic Heterogeneity

17. Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13

18. Interpretation of Genetic Linkage Findings

19. Possible localization of a major gene for cleft lip and palate to 4q

20. Gametic but not somatic instability of CAG repeat length in Huntington's disease

21. Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15

22. Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting

23. Software support for Huntingtons disease research

24. Genetics of Alcoholism

25. Genetic family history questionnaire

26. Contents, Vol. 22, 1978

27. Contents, Vol. 37, 1984

28. Identification of a new hereditary amyloidosis prealbumin variant, Tyr-77, and detection of the gene by DNA analysis

29. Anticipation in Huntington's disease is inherited through the male line but may originate in the female

30. Contents Vol. 40, 1985

31. Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis

32. Subject Index Vol. 22, 1978

33. Linkage analysis in a large kindred with autosomal dominant transmission of polyglandular autoimmune disease type II (Schmidt syndrome)

34. Genetic linkage map of human chromosome 21

35. Urinary pepsinogen isozymes: A highly polymorphic locus in man

36. Association of blood groups with essential and secondary hypertension. A possible association of the MNS system

38. Genetic Load Expressed as Fetal Death in Cattle

39. Linkage analysis in von Recklinghausen neurofibromatosis (NF1) with DNA markers for chromosome 17

40. Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22

41. Two models for a maternal factor in the inheritance of Huntington disease

42. DNA linkage analysis of X chromosome-linked chronic granulomatous disease

43. Pelizaeus-Merzbacher disease: tight linkage to proteolipid protein gene exon variant

44. Population genetic studies of retinitis pigmentosa

45. Genetic linkage between Huntington's disease and the DNA polymorphism G8 in South Wales families

46. The paradigm of Huntington disease

47. Huntington disease: genetics and epidemiology

48. Considerations in using linkage analysis as a presymptomatic test for Huntington's disease

49. A Medical Genetics Data Base Management System

50. Duffy blood group and hemoglobin variants

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