The Finnish population structure A genetic and genealogical study

Hereditas

Volumn 71, Issue 2, 1972, Pages 195-235

  NEVANLINNA, H R ^a  

^a FINNISH RED CROSS BLOOD SERVICE   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

PLASMA PROTEIN;

ARTICLE; BLOOD GROUP; CONSANGUINITY; DOMINANT GENE; ETHNOLOGY; FEMALE; FINLAND; GENE FREQUENCY; GENETIC POLYMORPHISM; HUMAN; MALE; POPULATION GENETICS; RECESSIVE GENE; RURAL POPULATION; SEX CHROMOSOME;

BLOOD GROUPS; BLOOD PROTEINS; CONSANGUINITY; FEMALE; FINLAND; GENE FREQUENCY; GENES, DOMINANT; GENES, RECESSIVE; GENETICS, POPULATION; HUMAN; MALE; POLYMORPHISM (GENETICS); RURAL POPULATION; SEX CHROMOSOMES;

EID: 0015436884     PISSN: 00180661     EISSN: 16015223     Source Type: Journal    
DOI: 10.1111/j.1601-5223.1972.tb01021.x     Document Type: Article

References (88)

1. Taste‐deficiency in Lappish and Finnish populations
2. Aspartylglucosaminuria. An analysis of thirty‐four patients
3. Transferrin variants in Lapps and Swedes
4. Discussion on polymorphism in man
5. A “new” Kell blood group phenotype
6. The pedigrees of two people already reported as of phenotype K‐, k‐, Kp(a‐b‐)
7. X‐chromosomal retinoschisis (retinal detachment) in Finland
8. X‐chromosomal recessive retinoschisis
9. Studien über Cornea plana congenita bei 19 Kranken in 9 Familien
10. Cornea plana congenita
11. a: Serological and physiochemical aspects
12. 12
13. a (Karhula)
14. 12‐malabsorption and proteinuria in young people
15. 12‐Malabsorption mit Proteinurie
16. The estimation and significance of the logarithm of a ratio of frequencies
17. Nephrotic syndrome in newborn and young infants
18. Myoclonus epilepsy (Unverricht‐Lundborg) in Finland
19. The measurement of taste sensitivity to phenylthiourea (P.T.C.)
20. Genetical studies on the Rh blood group system
21. Individual precipitation patterns of normal rabbit sera
22. Immune‐electrophoretic demonstration of qualitative differences in human sera and their relation to the haptoglobins
23. A simple method of determining haptoglobin groups in human sera by means of agar‐gel electrophoresis
24. Rare congenital coagulation defects in Finland
25. Congenital deficiency of fibrin stabilizing factor
26. Idiopathic chronic megaloblastic anemia in children
27. A study in the morphology of the Finns and its relation to the settlement of Finland
28. Familial protein intolerance with deficient transport of basic amino acids
29. Population genetic studies of the indigenous peoples of Australia and New Guinea
30. Chi in various populations
31. The red cell antigen Pk and its relationship to the P system: the evidence of three more families
32. Progressive myoclonus epilepsy
33. A general program for maximum likelihood estimation of gene frequencies
34. Congenitale chloride diarrhoea and lactose malabsorption
35. Disaccharidases and histology of duodenal mucosa in congenital lactose malabsorption
36. Familial chloride diarrhoea‐chloride malabsorption
37. A matching problem arising in genetics
38. Hypothyroidism with defective organic binding of iodide
39. Inherited defects in the metabolism of thyroid hormones
40. A “new” antigen and antibody belonging to the Pk blood group system
41. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms
42. Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation
43. Transferrin variation in Columbidae
44. The distribution of blood and serum groups in a Finnish population living around Leningrad (Ingria) through ten generations
45. The heredity of congenital nephrosis
46. Heredity in the congenital nephrotic syndrome
47. The nephrotic syndrome and heredity
48. Dystrophia retinae pigmentosa‐dysacusis syndrome (DRD): a study of the Usher or Hallgren syndrome
49. Prevalence of phenylketonuria and some other metabolic disorders among mentally retarded patients in Finland
50. Aspartylglucosaminuria
51. Eleven new cases of aspartylglucosaminuria
52. Further cases of aspartylglucosaminuria
53. Non‐parasitic cysts of the liver: a clinical study of 117 cases
54. Cardilage‐hair hypoplacia, diastrophic nanism, and mulibrey nanism
55. Hereditary fructose intolerance, galactosaemia and the glycogenoses
56. Congenital adrenal hyperplacia, and the syndrome of hypoparathyroidism, Addisons disease and candidiasis
57. Aspartylglucosaminuria. An inborn error of metabolism associated with mental defect
58. Rh chromosome frequencies in England
59. Comparison of genetical and morphological methods for a study of biological differences
60. Distribution of serum transferrin groups in Finland and their inheritance
61. Blodgruppsfördelningen bland svensktalande i Finland
62. Clinical findings in three patients with non‐ketocic hyperglycinaemia
63. Zone electrophoresis in starch gels: groups variations in the serum proteins of normal human adults
64. Blutgruppenforschung und Anthropologie
65. Hereditary X‐linked retinoschisis in the region of Pori
66. Inborn errors of amino acid metabolism
67. Screening of newborns for PKU in Finland