Haplotype analysis of congenital nephrotic syndrome of the Finnish type in non-Finnish families

Journal of the American Society of Nephrology

Volumn 7, Issue 12, 1996, Pages 2700-2703

  Männikkö, Minna ^a   Lenkkeri, Ulla ^a   Kashtan, Clifford E ^b   Kestilä, Marjo ^a   Holmberg, Christer ^c   Tryggvason, Karl ^a,d  

^a UNIVERSITY OF OULU   (Finland)

^b UNIVERSITY OF MINNESOTA MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF HELSINKI   (Finland)

^d KAROLINSKA INSTITUTE   (Sweden)

Author keywords

Chromosome 19; Founder effect; Genetic typing; Linkage; Linkage disequilibrium

Indexed keywords

ARTICLE; CHROMOSOME 19Q; CONGENITAL NEPHROTIC SYNDROME; FAMILY STUDY; FEMALE; FINLAND; GENE LOCUS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC MARKER; HAPLOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL;

EID: 0030391720     PISSN: 10466673     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. Huttunen NP: Congenital nephrotic syndrome of Finnish type: Study of 75 patients. Arch Dis Child 1976;51:344-348.
2. Norio R, Nevanlinna HR, Perheentupa J: Hereditary diseases in Finland: Rare flora in rare soil. Ann Clin Res 1973;5:109-141.
3. de la Chapelle A: Disease gene mapping in isolated human populations: The example of Finland. J Med Genet 1993;30:857-865.
4. Nevanlinna HR: The Finnish population structure: A genetic and genealogical study. Hereditas 1972;71:195-236.
5. Kestila M, Männikkö M, Holmberg C, et al.: Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19. Am J Hum Genet 1994;54:757-764.
6. Männikkö M, Kestilä M, Holmberg R, et al.: Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1. Am J Hum Genet 1995;57:1377-1383.
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8. Mahan JD, Mauer SM, Sibley RK, Vernier RL: Congenital nephrotic syndrome: Evolution of medical management of results of renal transplantation. J Pediatr 1984;105: 549-557